RN Pediatric Full-time
Arkansas Children's

Clinical Research Nurse Coordinator

apartment Arkansas Children's location_onLittle Rock, AR
ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS. This position has been designated as safety sensitive and cannot be filled by a candidate who is a current user of medical marijuana. CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account ( https://www.myworkday.com/archildrens/ )and search the "Find Jobs" report. Work Shift: Please see job description for details. Time Type: Full time Department: CC033021 Neurology Clinical Research Operations Summary: Additional Information: The Clinical Research Nurse Coordinator coordinates of clinical research studies. Serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study. The Clinical Research Nurse upholds standards for human subjects protection. Required Education: Associate Degree or Equivalent Experience Recommended Education: Bachelor's Degree Required Work Experience: Related Field - 3 years of experience Recommended Work Experience: Required Certifications: Registered Nurse (RN) license - Arkansas or Compact State Recommended Certifications: Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates Description 1. Prepares materials for approval by ACRI and the applicable IRB. 2. Conducts screening procedures for study enrollment. Recruits subject for participation and obtains consent/assent for research participation. 3. Prepares flowcharts, study specific source documents and other study related materials. 4. Assures clinical interventions are administered per protocol. 5. Collects/records subject data on the case report forms using source documentation. 6. Serve as a clinical/research resource to subjects, families, and other healthcare providers regarding the needs of the study and subject/family. 7. Collaborates with other caregivers, research team members, and subject/family in planning, implementing, and evaluating research activities. 8. Performs other duties as assigned.
RN Full-time
Cedars-Sinai

Research Nurse Coordinator I (Hybrid)

apartment Cedars-Sinai location_onBeverly Hills, CA
Job Description The Research Nurse Coordinator I is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfaces with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who provide hands-on clinical care to research participants. Utilizes clinical nursing background and basic research protocol knowledge to serve as a liaison between nursing staff, Principal Investigator, other research staff, and study participants. Primary Duties and Responsibilities Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff. Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process. Assesses and documents adverse events reported by research participants, informs PI, and documents according to department process (grade, attribution, treatment, etc), and reports to regulatory and sponsor as required. Records research data where assessed or reported by patient (i.e. symptoms of treatment). Presents education materials to the interdisciplinary team on study requirements. Collaborates with the interdisciplinary team and communicate a plan of care that allows for safe and effective collection of clinical research data. Schedules research participant study visits. Triages patient by phone and provides clinical information to the patient. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities. Coordinates study participant tests and/or procedures as required and ensures protocol is followed. May prepare IRB submissions. May process, ship, track or otherwise handle research specimens. Qualifications Required: Associate. Degree/College Diploma Nursing required. 2 years of Clinical Nursing Experience required. RN State License California RN license Upon Hire. Basic Life Support Upon Hire. Preferred: Bachelor's Degree Nursing or Health Science preferred. 1 year Clinical research experience preferred. Req ID : 14260 Working Title : Research Nurse Coordinator I (Hybrid) Department : Cancer - SOCCI Clinical Research Business Entity : Cedars-Sinai Medical Center Job Category : Nursing Job Specialty : Research Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $40.03 - $60.05
RN Full-time
MUSC

Cellular Therapy RN Coordinator

apartment MUSC location_onCharleston, SC
Job Description Summary The Clinical Cellular Therapy / IEC RN Coordinator II reports to the HCC BMT/IEC Program Director. Under general supervision, the Clinical RN Coordinator II develops and uses advanced clinical management, consultation, education and research to promote quality care for the specific transplant patient populations. Provides growth in a clinical knowledge through research based practice with peers. Entity Medical University Hospital Authority (MUHA) Worker Type Employee Worker Sub-Type​ Regular Cost Center CC000283 CHS - Bone Marrow Transplant Pay Rate Type Salary Pay Grade Health-29 Scheduled Weekly Hours 40 Work Shift Job Description The Clinical Cellular Therapy / IEC RN Coordinator II reports to the HCC BMT/IEC Program Director. Under general supervision, the Clinical RN Coordinator II develops and uses advanced clinical management, consultation, education and research to promote quality care for the specific transplant patient populations. Provides growth in a clinical knowledge through research based practice with peers. Additional Job Description Bachelor's degree in Nursing from an accredited school of nursing and a minimum of three years related clinical nursing work experience required. Licensure a registered nurse by the South Carolina Board of Nursing or compact state required. Certification as a generalist in a related specialty area by the American Nurses Association (ANA) preferred. Current American Heart Association (AHA) Basic Life Support (BLS) certification or American Red Cross BLS for Healthcare Providers certification is required If you like working with energetic enthusiastic individuals, you will enjoy your career with us! The Medical University of South Carolina is an Equal Opportunity Employer. MUSC does not discriminate on the basis of race, color, religion or belief, age, sex, national origin, gender identity, sexual orientation, disability, protected veteran status, family or parental status, or any other status protected by state laws and/or federal regulations. All qualified applicants are encouraged to apply and will receive consideration for employment based upon applicable qualifications, merit and business need. Medical University of South Carolina participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here: http://www.uscis.gov/e-verify/employees
RN Manager/Supervisor Other
MaineHealth

Supervisor - Research Nurse Coordinator/RN - MaineHealth Institute for Research

apartment MaineHealth location_onScarborough, ME
Description Management/Leadership Req #: 59494 Summary This position is for someone interested in joining a hands-on team at the MaineHealth Institute for Research. This Research Nurse Coordinator Supervisor will work at the direction of the Manager, Clinical Trials Office, playing a key role in the delivery of our Oncology therapeutic clinical trials mission to provide the highest quality research conduct and the best experience possible to our research participants. This role will serve as an educational resource to nurses conducting clinical research studies, supervising staff, overseeing training and ongoing operational support of Oncology Research Nurse Coordinators. A hybrid work schedule from our Scarborough, Maine location is available for this position. Aresume or CV AND Cover Letter are required to be considered for this position. Learn more about the MaineHealth Institute for Research in this short video! Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: See "License/Certifications" License/Certifications: Current license to practice as a Registered Nurse in the State of Maine.Current Clinical Research Coordinator Certification (ACRP or SOCRA) required. Experience: 5+ years of research experience is required. MH research experience is preferred. Thorough knowledge of theory, practice, principles, processes and issues of nursing usually acquired through 2-3 years of clinical experience. Additional Skills/Requirements Required: Demonstrated ability to serve in a role as a leader or a mentor. Ability to manage complex projects through all phases of development, implementation, and follow-up. Additional Skills/Requirements Preferred: N/A Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact lauren.robare@mainehealth.org
RN Full-time
Riverside Health System

RN Clinical Research

apartment Riverside Health System location_onLexington, KY
Newport News, Virginia Overview Performs duties related to the conduct of clinical trials in accordance with RHS policies, protocol requirements as well as all local, state, and federal regulations/guidelines. Works closely with the Principle Investigator (PI), members of the research team, physicians, study sponsors and monitors and IRB (Internal Review Board) to provide guidance on administration of the compliance, financial, contracts, and other regulatory aspects of clinical studies. Manages and coordinates all aspects of conducting clinical trials within Riverside Health System. What you will do Maintains frequent open communication with PI and Clinical Research Coordinator on all protocol requirements and regulatory responsibilities. Demonstrates ability to build trusting collaborative relationships with patients and families to facilitate subject retention. Addresses concerns and resolves conflict directly and professionally in a respectful manner. Assists in the contract/budget negotiation process. Maintains accurate financial records to ensure proper billing and accounting for all trial related services and activities. Enters data into CTMS accurately and in a timely manner. Submission of study related activities are completed and timely. Coordinates multiple clinical trials simultaneously or clinical trials with unique complexity. Maintains all required documentation for monitors and according to regulatory guidelines. Ensures all clinical trials are executed in compliance with ICH/GCP guidelines, regulations, and standard operating procedures. Maintains all clinical trial documentation according to guidelines. Ensures the randomization procedures, and blinding procedures, if applicable, are followed as per protocol guidelines. Works in collaboration with PI and Physicians on prescreening through the electronic health record for potential subjects to participate in the clinical trials. Participates and supports all sites auditing and monitoring visits. Promptly reports all protocol variances to appropriate parties. Provides equitable and confidential treatment to all patients throughout the clinical trial. Adheres to HIPAA policies to maintain patient confidentiality. In collaboration with Principle Investigator, Clinical Research Coordinator is responsible for initiating the Informed Consent (ICF) process and ensures that no study related procedures are performed prior to obtaining ICF. Reviews study protocols and demonstrates knowledge of all procedures and requirements. Assures the integrity and quality of clinical research trial is maintained and conducted in accordance with Good Clinical Practice/ICH guidelines. Ensures adherence to the protocol, schedule of events, and other requirements. Prepares source documents specific to the studies. Assures quality, completeness, and verifies accuracy of source documents and case report forms collected during the course of the study. Ensures information is recorded on case report forms and resolves queries in a timely manner. Provides education for patients and families about all aspects of study protocol during all phases from screening through follow-up and closure of the study. Prepares all specimens as required by the protocol and adheres to (International Air Transport Association) IATA guidelines. Maintains accountability for Investigational Product (IP). Prepares and dispenses IP (oral form only can be administered by CRC) per protocol Stores all files in a permanent and safe location. Gathers and records all required study related to the Clinical Trial Management System (CTMS). Reports all Serious Adverse Events (SAE) to the Principle Investigator, monitor, sponsor, and IRB as required. Assesses and records all Adverse Events as outlined in protocol. Reports all Serious Safety Events (SAEs) in collaboration with Clinical Research Coordinator to the Principle Investigator, Monitor, Sponsor, and IRB as required. Works in collaboration with Investigators and Clinical Research Coordinators to verify eligibility and feasibility of potential trial subjects according to the inclusion/exclusion criteria. Prescreens through the electronic medical record for potential subjects. Disseminates IRB approved recruitment materials. Assesses, documents and reports adverse events (AE) to PI and ensure appropriate follow up as required. Prompt notification to IRB/sponsor of any AE classified as serious or unexpected. Ensures PI acknowledgment of all safety reports, abnormal test results in a timely manner. Adheres to all Human Subject protection guidelines. Attends all training sessions related to clinical trials to include Investigator meetings, site initiation visits, and all training related to the conduct of the Trial. Works in collaboration with the Clinical Research Coordinator in providing education for all study staff and ancillary departments. Instructs patient on the proper usage of investigational product/device. Maintains open communication with subjects to ensure adherence to protocol requirements. Supports orientation and training of new research team members and other team members with Riverside Health System. Qualifications Education Bachelors Degree, Nursing (Preferred) Experience 2 years Clinical research or clinical trial coordination experience (Preferred) Licenses and Certifications Registered Nurse (RN) - Virginia Department of Health Professions (VDHP) Upon Hire(Required) Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals (Preferred) International Air Transport Association (IATA) (Preferred) Collaborative Institutional Training Initiative (CITI) (Preferred) To learn more about being a team member with Riverside Health System visit us at https://www.riversideonline.com/careers .
RN Other
MaineHealth

Clinical Research Nurse Coordinator (RN) - Cardiology

apartment MaineHealth location_onPortland, ME
Description Nursing Req #: 49923 This is a bargaining unit position Date Posted: 11/4/2025 FT/Days/Varies THIS POSITON REQUIRES A REGISTERED NURSE LICENSE** Maine Medical Center’s Cardiology Service Team is seeking a Research Nurse Coordinator. The RN joining this team will be part of a strategic initiative to help develop a Cardiovascular Research Center. The Selected Candidate Will Be Responsible For Understanding the clinical trials protocols Identifying patients to participate in the study Explaining the protocols and educatingthe patient Schedule : This position offers a schedule primarily consisting of days. Availability to work early morning or evenings is required as cases arise. On occasion, weekends may be required. Summary The Clinical Research Nurse Coordinator role is responsible for coordinating research activities within the assigned department. Oversees the conduct of research studies including developing research protocols, determining participant eligibility, obtaining informed consent, and conducting necessary follow-up with study participants. Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: Bachelor's Degree in a health science field required. Master’s Degree preferred. License/Certifications: Current applicable state license as a Registered Nurse required. Experience: Two years of clinical experience in a healthcare setting required. 4+ years of cardiology experience preferred. Cardiac procedure experience (interventional cardiology, electrophysiology, cardiac surgery) strongly preferred. Additional Skills/Requirements Required: N/A Additional Skills/Requirements Preferred: N/A Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact nicole.chapman@mainehealth.org
RN Full-time
Florida Cancer Specialists & Research Institute

Clinical Research Coordinator III RN

apartment Florida Cancer Specialists & Research Institute location_onWest Palm Beach, FL
Date Posted: 2025-12-08 Country: United States of America Location: Palm Beach Gardens Office WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. Offering competitive salaries and comprehensive benefits packages to include tuition reimbursement, 401-K match, pet and legal insurance. A LITTLE BIT ABOUT FCS Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Often, FCS leads the nation in initiating research studies and offering ground-breaking new therapies to patients. Come join us today! RESPONSIBILITIES Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director. The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies. May be responsible for providing coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III. QUALIFICATIONS Candidates must have a valid RN license, in state of employment, a minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience. Candidates must have effective communication skills, be organized, detail oriented, strong patient advocates. Candidates must be available to travel to investigators meetings. Valid Driver’s License, in state of residency, for travel to clinics. Must comply with the Company’s Driver Safety Operations and Motor Vehicle Records Check Pol #LI-DL1 SCREENINGS – Background, drug, and nicotine screens Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized. EEOC Florida Cancer Specialists & Research Institute (FCS) is committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at FCS, please email FCS Recruitment ( Recruiter@FLCancer.com ) for further assistance. Please note this email address is intended to request an accommodation as part of the application process. Any other correspondence will not receive a response. FCS is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
RN Full-time
Florida Cancer Specialists & Research Institute

Clinical Research Coordinator III RN

apartment Florida Cancer Specialists & Research Institute location_onSarasota, FL
Date Posted: 2025-12-08 Country: United States of America Location: Research Cattlemen WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. Offering competitive salaries and comprehensive benefits packages to include tuition reimbursement, 401-K match, pet and legal insurance. A LITTLE BIT ABOUT FCS Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Often, FCS leads the nation in initiating research studies and offering ground-breaking new therapies to patients. Come join us today! RESPONSIBILITIES Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director. The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies. May be responsible for providing coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III. QUALIFICATIONS Candidates must have a valid RN license, in state of employment, a minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience. Candidates must have effective communication skills, be organized, detail oriented, strong patient advocates. Candidates must be available to travel to investigator meetings. Valid Driver’s License, in state of residency, for travel to clinics. Must comply with the Company’s Driver Safety Operations and Motor Vehicle Records Check Pol #LI-DL1 SCREENINGS – Background, drug, and nicotine screens Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized. EEOC Florida Cancer Specialists & Research Institute (FCS) is committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at FCS, please email FCS Recruitment ( Recruiter@FLCancer.com ) for further assistance. Please note this email address is intended to request an accommodation as part of the application process. Any other correspondence will not receive a response. FCS is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
RN Full-time
Florida Cancer Specialists & Research Institute

Clinical Research Coordinator III RN

apartment Florida Cancer Specialists & Research Institute location_onWest Palm Beach, FL
Date Posted: 2025-10-17 Country: United States of America Location: Palm Beach Gardens Office WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. Offering competitive salaries and comprehensive benefits packages to include tuition reimbursement, 401-K match, pet and legal insurance. A LITTLE BIT ABOUT FCS Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Often, FCS leads the nation in initiating research studies and offering ground-breaking new therapies to patients. Come join us today! RESPONSIBILITIES Responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director. The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies. May be responsible for providing coverage in clinics when research staff are out of the office; for precepting new research staff in clinics; for assisting with research projects assigned by the Senior Clinical Research Coordinator III. QUALIFICATIONS Candidates must have a valid RN license, in state of employment, a minimum of one-year oncology or clinical research experience; or a minimum of five years of combined clinical oncology and clinical research experience. Candidates must have effective communication skills, be organized, detail oriented, strong patient advocates. Candidates must be available to travel to investigators meetings. Valid Driver’s License, in state of residency, for travel to clinics. Must comply with the Company’s Driver Safety Operations and Motor Vehicle Records Check Pol SCREENINGS – Background, drug, and nicotine screens Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized. EEOC Florida Cancer Specialists & Research Institute (FCS) is committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at FCS, please email FCS Recruitment ( Recruiter@FLCancer.com ) for further assistance. Please note this email address is intended to request an accommodation as part of the application process. Any other correspondence will not receive a response. FCS is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
RN Oncology Full-time
Cedars-Sinai

Research Nurse Coordinator II (Hybrid), Neuro-Oncology

apartment Cedars-Sinai location_onBeverly Hills, CA
Job Description This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. Hybrid schedule is 3 days a week onsite, 2 days remote. Standard hours 8:00am – 4:30pm. No expectation around weekend work. You will play a vital part in supporting clinical research with Phase I investigators and the Neuro-Oncology Disease Research Group (DRG). This position offers the opportunity to collaborate closely with a multidisciplinary team while contributing to innovative therapies and patient care. The RNC II will take ownership of a wide range of research activities — from conducting detailed protocol assessments and performing intradermal injections, to educating patients, providing nursing in-services, reporting SAEs/DLTs, and supporting screening and enrollment processes. This role will also support essential operational tasks such as coordinating research visits, assisting with research billing inquiries, and ensuring flow sheets and study requirements are accurately followed. As part of the larger Phase I team, the RNC II will also contribute to the ongoing success of the Neuro-Oncology DRG, helping drive meaningful research that impacts patient outcomes. The Research Nurse Coordinator II is responsible for all activities associated with clinical study coordination, subject recruitment/enrollment, data management/integrity, regulatory compliance, project/study evaluation and interfacing with participants and family members. Coordinates the clinical logistics of the study, and works in tandem with the Research and/or Clinical Nurse who work to provide hands-on clinical care to research participants. Utilizes clinical nursing background and extensive research protocol knowledge to serve as a liaison between nursing staff, Principal Investigator, other research staff, and study participants. Assists with the education of staff, and provides general oversight of research portfolio as it pertains to the clinical coordination of the studies. Primary Duties and Responsibilities Responsible for clinical study activities, coordination, adherence to protocols and serves as a liaison between study participants, Principal Investigator (PI), and other research staff. Provides educational services to research participants and family regarding study participation, participants current clinical condition, and or disease process. Assesses and documents adverse events as reported by research participants, works closely with PI to document according to department process (grade, attribution, treatment, etc.), and reports to regulatory and sponsor as required. Records research data where assessed or reported by patient (i.e. symptoms of treatment). Creates and presents education materials to the interdisciplinary team on study requirements. Collaborates with the interdisciplinary team to create and communicate a plan of care that allows for safe and effective collection of clinical research data. Triages patient by phone and provides clinical information to the patient. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities and ensures protocol is followed. Coordinates study participant tests and procedures as required. Prepares data spreadsheets for Investigator and/or department. Performs oversight of research portfolio as it pertains to the clinical coordination of the studies. Assists with the education of staff. May assist with grant proposals, publication preparation, and presentations. May process, ship, track or otherwise handle research specimens. Qualifications This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area. Requirements: Associate Degree/College Diploma required. Bachelors Degree preferred. Minimum of 3 years of clinical nursing experience, demonstrating strong clinical judgment, patient care skills, and the ability to work independently within a fast-paced healthcare environment. At least 2 years of clinical research experience, supporting protocol execution, patient enrollment, documentation, and regulatory compliance. Candidates must hold a current, valid California Registered Nurse (RN) license in good standing Req ID : 13286 Working Title : Research Nurse Coordinator II (Hybrid), Neuro-Oncology Department : Cancer - SOCCI Clinical Research Business Entity : Cedars-Sinai Medical Center Job Category : Nursing Job Specialty : Research Overtime Status : NONEXEMPT Primary Shift : Day Shift Duration : 8 hour Base Pay : $45.45 - $72.72
RN Full-time
Northwestern Medicine

Clinical Research Nurse Coordinator-Bluhm Cardiovascular Institute Full-time Days

apartment Northwestern Medicine location_onChicago, IL
Description The Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator initiated trials, sponsor trials) and Northwestern Medicine; a joint collaboration between NMG and the NU Feinberg School of Medicine. The Clinical Research Nurse Coordinator (CRNC) works collaboratively with the inter-professional team and peers to ensure appropriate implementation and conduct of clinical research studies throughout the lifecycle of a protocol. The CRNC adheres to the ANA Scope and Standards of Practice of Professional Nursing and the Code of Ethics. The CRNC utilizes the NIH Clinical Research Nurse Domain of Practice and Model of Care. The CRNC reflects the mission, vision, and values of Northwestern Medicine, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. Hours: Monday-Friday 8:00am-4:30pm Responsibilities: Leads the coordination and support to Principal Investigator(s). Reviews research studies in pre-submission phase for feasibility of protocol implementation. Guides the review, revision, and maintenance of protocols. Assures established protocols meet compliance and regulatory requirements. Provides guidance to clinical research nurses on projects related to new research study submissions, utilization reviews, wording/phrasing of medical orders, protocols and workflows. Develops and maintains clinical nursing research policies, standard operating procedures, and guidelines. Reviews and trends research-related deviations and workflow events, reports findings to the Manager and Inter-professional Quality Committee, and recommends action to ensure compliance. Supports the development of projects created in response to research-related problems and events as identified and reported by staff and research study team members (e.g., events, deviations, corrective and preventative actions). Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to orient and train new staff to clinical research. Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to identify training needed for clinical research nurses about unfamiliar practices, procedures and medications to ensure patient/subject safety and compliance with protocols and regulatory requirements. Escalates research-related concerns to the appropriate leader or committee. Serves as a mentor and role model for communication and collaboration with investigator teams and clinical and technical research practices. Supports the clinical research nursing staff during adverse events, emergencies, and difficult clinical situations. Provides clinical nursing support to both inpatient and/or outpatient teams as needed as a cross trained resource. Qualifications Required: Current license as a Registered Nurse in the State of Illinois. Experience in clinical trials BSN Minimum of two years related clinical experience. CPR-BLS Certification through the American Heart Association (AHA) Preferred: MSN Membership in Professional Nursing Organization ACLS Certification in clinical areas where required Society of Clinical Research Associates' (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification Certification in area of clinical specialty. Equal Opportunity Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status. Background Check Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check. Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act. Artificial Intelligence Disclosure Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person. Benefits We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section to learn more. Sign-on Bonus Eligibility: Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.
RN Full-time
Baptist Memorial Health Care

Coordinator-Research Nurse I RN

apartment Baptist Memorial Health Care location_onMemphis, TN
Overview Job Summary The Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, assuring that the integrity and quality of the research is maintained and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal, and sponsor regulations and guidelines, BMHCC and BCRI policies and procedures. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up. This position may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. This position will collaborate with research coordinators, data managers and regulatory specialists. Travel may be required. Responsibilities Facilitates compliance with the requirements of the research protocol and good clinical practice while remaining cognizant of the needs of diverse patient populations. Communicates with research team to facilitate the effective conduct of clinical trials. Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions. Manages the activities of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements. Ensures collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial. Enhances recruitment while being mindful of the needs of diverse patient populations. Enhances adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data. Identifies financial variables that affect research and supports good financial stewardship in clinical trials. Identifies his or her ongoing professional development needs and seeks resources and opportunities to meet those needs, such as memberships in nursing, oncology, or research organizations. Other responsibilities as assigned. Specifications Experience Minimum Required 2 years of Research or Clinical experience Preferred/Desired 2 years of Oncology or Clinical Research Experience Education Minimum Required Currently licensed nurse or equivalent combination of education and experience Preferred/Desired Preferred/Desired bachelors degree in Nursing. Training Minimum Required Preferred/Desired Special Skills Minimum Required Preferred/Desired Computer skills to include MS Word, Excellent organizational skills. Detail oriented. Experience with EMR and Clinical Trial Management System Licensure Minimum Required BLS certification within 14 days; RN License required by state. Preferred/Desired Certifications - SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals), Collaborative Institutional Training Initiative (CITI), HAZMAT, CCRP or CCRC
RN Full-time
University of Kansas Medical Center

Clinical Research Nurse Coordinator - Internal Medicine (Endocrinology, Diabetes & Clinical Pharmacology)

apartment University of Kansas Medical Center location_onKansas City, MO
$65,000 - $99,000 / YEAR
Department: SOM KC The Diabetes Institute (DI) ----- Diabetes Institute Position Title: Clinical Research Nurse Coordinator - Internal Medicine (Endocrinology, Diabetes & Clinical Pharmacology) Job Family Group: Professional Staff Job Description Summary: The Clinical Research Nurse Coordinator in the Diabetes Institute manages clinical research studies by coordinating and participating in a variety of complex activities involved in the collection, compilation, documentation, and analysis of clinical research data. This role monitors participant progress, including documenting and reporting adverse events, and participates in periodic quality assurance audits of study protocols. The position provides professional nursing care and patient monitoring for clinical trials and works collaboratively with multidisciplinary teams, research personnel, and hospital staff to recruit, screen, educate, and support participants throughout the clinical study coordination process. The KU Diabetes Institute's mission is to advance research leading toward prevention and control of diabetes, as well as an eventual cure for the disease. Researchers and clinicians from the University of Kansas Medical Center, the University of Kansas-Lawrence, and the KU School of Medicine-Wichita form the core of the Institute and are engaged in a wide range of basic science, translational and clinical research projects centering around diabetes and its complications. Job Description: Job Duties Plan, provide, and document professional nursing care utilizing the nursing process for patients in accordance with physician orders, institutional SOPs, and state licensure scope of practice. Assure that all professional nursing care provided is conducted in accordance with all KUMC and other regulatory requirements and is in accordance with the scope of practice for the nursing license held. Recruit, educate potential patients for and evaluate potential patient eligibility for clinical trials seeking guidance from Clinical Research Supervisor. Assist clinical staff with maintaining source documents and submit case report forms (CRFs) as required for clinical trials. Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors. Perform study procedures, as outlined in the protocol and within state and institutional scope of practice. Perform phlebotomy and sample collection, processing, handling, and shipping as outlined in the protocol and within KUMC policy. Ensure adequate study supplies are being maintained. Track study expenditures and submit reimbursement requests for study equipment, supplies, and study participants. Prepare documentation and participate in study monitoring visits, reviews, and audits. Provide written and verbal reports to Principal Investigator and Project Manager, as required. Attend continuing education, research and training seminars as requested by manager. Participate in quality assurance activities by reviewing clinical data in medical record charts, assessing pharmacy compliance with protocol criteria, and reviewing study documentation to ensure compliance with GCP guidelines and FDA CFR. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job, not an exhaustive list of all possible job responsibilities, tasks, duties, and assignments. Furthermore, job duties, responsibilities and activities may change at any time with or without notice. Work Environment: This role will be fully on-site. Required Qualifications Certifications/Licenses: Registered Nurse license. Work Experience: 2 years of related work experience. Experience with regulations governing clinical research (CFR, GCP, HIPAA). Experience with statutes and guidelines relevant to regulatory affairs in clinical research. Experience with study budgets, contracts, and grant applications. Preferred Qualifications Education: Bachelor of Science Nursing (RN-BSN) Certifications: Certified Clinical Research Coordinator (CCRC) or certification eligible Certified Clinical Research Professional (CCRP) or certification eligible. Healthcare certifications preferred such as Basic Life Support (BLS) or Advanced Cardiac Life Support (ACLS) within 3 months of employment. Work Experience: Supervisory experience. Skills Communication Presentation skills Organization Multitasking Interpersonal skills Time management Required Documents Resume/CV Cover letter Comprehensive Benefits Package: Coverage begins on day one for health, dental, and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans are available. Paid time off, including vacation and sick, begins accruing upon hire, plus ten paid holidays. One paid discretionary day is available after six months of employment, and paid time off for bereavement, jury duty, military service, and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. https://www.kumc.edu/human-resources/benefits.html Employee Type: Regular Time Type: Full time Rate Type: Salary Compensation Statement: The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including, but not limited to, education, experience and training, qualifications relative to the requirements of the position, and funding. At the University of Kansas Medical Center, a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range, taking into account the combination of factors listed above. Pay Range: $65,000.00 - $99,000.00 Minimum $65,000.00 Midpoint $82,000.00 Maximum $99,000.00
RN Full-time
Northwestern Medicine

Registered Nurse Clinical Research Nurse Coordinator-Bluhm Cardiovascular Institute Full-time Days

apartment Northwestern Medicine location_onChicago, IL
Description The Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams (e.g., investigator initiated trials, sponsor trials) and Northwestern Medicine; a joint collaboration between NMG and the NU Feinberg School of Medicine. The Clinical Research Nurse Coordinator (CRNC) works collaboratively with the inter-professional team and peers to ensure appropriate implementation and conduct of clinical research studies throughout the lifecycle of a protocol. The CRNC adheres to the ANA Scope and Standards of Practice of Professional Nursing and the Code of Ethics. The CRNC utilizes the NIH Clinical Research Nurse Domain of Practice and Model of Care. The CRNC reflects the mission, vision, and values of Northwestern Medicine, adheres to the organization’s Code of Ethics and Corporate Compliance Program, and complies with all relevant policies, procedures, guidelines and all other regulatory and accreditation standards. Collaborate with a wide range of professionals to disseminate patient care outcomes through publications and presentations, managing all stages of research projects—from feasibility, project conception and approval, data collection, literature review to manuscript submission. Participates in monthly meetings with surgeons and NU research team staff to track progress of projects. Clinical expertise in cardiac surgery (valve and atrial fibrillation procedures) is preferred. Hours: Monday-Friday 8:00am-4:30pm Responsibilities: Leads the coordination and support to Principal Investigator(s). Reviews research studies in pre-submission phase for feasibility of protocol implementation. Guides the review, revision, and maintenance of protocols. Assures established protocols meet compliance and regulatory requirements. Provides guidance to clinical research nurses on projects related to new research study submissions, utilization reviews, wording/phrasing of medical orders, protocols and workflows. Develops and maintains clinical nursing research policies, standard operating procedures, and guidelines. Supports the development of projects created in response to research-related problems and events as identified and reported by staff and research study team members (e.g., events, deviations, corrective and preventative actions). Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to orient and train new staff to clinical research. Collaborates with Clinical Coordinators, Education Coordinators, and peer CRNCs to identify training needed for clinical research nurses about unfamiliar practices, procedures and medications to ensure patient/subject safety and compliance with protocols and regulatory requirements. Escalates research-related concerns to the appropriate leader or committee. Serves as a mentor and role model for communication and collaboration with investigator teams and clinical and technical research practices. Supports the clinical research nursing staff during adverse events, emergencies, and difficult clinical situations. Provides clinical nursing support to both inpatient and/or outpatient teams as needed as a cross trained resource. Qualifications Required: Current license as a Registered Nurse in the State of Illinois. Experience in clinical trials BSN Minimum of two years related clinical experience. CPR-BLS Certification through the American Heart Association (AHA) Preferred: MSN Membership in Professional Nursing Organization ACLS Certification in clinical areas where required Society of Clinical Research Associates' (SOCRA) or Association of Clinical Research Professionals (ACRP) Certification Certification in area of clinical specialty. Equal Opportunity Northwestern Medicine is an equal opportunity employer (disability, VETS) and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, disability, sexual orientation or any other protected status. Background Check Northwestern Medicine conducts a background check that includes criminal history on newly hired team members and, at times, internal transfers. If you are offered a position with us, you will be required to complete an authorization and disclosure form that gives Northwestern Medicine permission to run the background check. Results are evaluated on a case-by-case basis, and we follow all local, state, and federal laws, including the Illinois Health Care Worker Background Check Act. Artificial Intelligence Disclosure Artificial Intelligence (AI) tools may be used in some portions of the candidate review process for this position, however, all employment decisions will be made by a person. Benefits We offer a wide range of benefits that provide employees with tools and resources to improve their physical, emotional, and financial well-being while providing protection for unexpected life events. Please visit our Benefits section to learn more. Sign-on Bonus Eligibility: Internal employees and rehires who left Northwestern Medicine within 1 year are not eligible for the sign on bonus. Exception: New graduate internal employees seeking their first licensed clinical position at NM may be eligible depending upon the job family.
RN Other
MaineHealth

Clinical Research Nurse Coordinator - MaineHealth Institute for Research

apartment MaineHealth location_onRockport, ME
Description MaineHealth Institute for Research Nursing Req #: 55856 Summary The Clinical Research Nurse Coordinator role is responsible for coordinating research activities within the assigned department. Oversees the conduct of research studies including developing research protocols, determining participant eligibility, obtaining informed consent, and conducting necessary follow-up with study participants. Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: Bachelor's Degree in a health science field required. Master’s Degree preferred. License/Certifications: Current applicable state license as a Registered Nurse required. Experience: Two years of clinical experience in a healthcare setting required. Additional Skills/Requirements Required: N/A Additional Skills/Requirements Preferred: N/A Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact lauren.robare@mainehealth.org Show more Show less
RN Pediatric Full-time
Driscoll Children's Hospital

Transport RN Coordinator

apartment Driscoll Children's Hospital location_onCorpus Christi, TX
Where compassion meets innovation and technology and our employees are family. Thank you for your interest in joining our team! Please review the job information below. Transport Coordinator Through research and evidence-based practice, guides and establishes clinical best practice for the Transport Program. The Transport Clinical Coordinator serves as a key resource to medical team members on clinical matters. He/she is directly responsible to assure all training, and certifications meet or exceed standards, gathers relevant quality data to trend clinical demands, deficiencies, and develops related education and training to improve overall clinical practice. The Transport Clinical Coordinator works directly with physician medical directors, and primary receiving physicians, to measure clinical outcomes and performance improvements. He/she is cross trained in neonatal and pediatric care and meets the requirements of the Transport Coordinator duties as outlined in this job description. The Transport Clinical Coordinator reports directly to the Transport Director and works closely with peer Coordinators. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description is not intended to be all-inclusive; employees will perform other reasonably related business duties as assigned by the immediate supervisor and/or hospital administration as required. Maintains utmost level of confidentiality at all times. Adheres to hospital policies and procedures. Demonstrates business practices and personal actions that are ethical and adhere to corporate compliance and integrity guidelines. Identifies essential relationships and/or sees the variations in clinical patterns for Neonatal, Pediatric, and Adult patient populations. Displays intuitive grasp of patient’s status, based on broad knowledge base and expertise. Evaluates clinical practice and follows through with modifications, procedure and clinical guidelines that reflect evidence-based and research-based best practice. Participates actively in process improvement, transport education, and research activities. Complies with and integrates institutional and regulatory standard into clinical practice. Attends all transport departmental meetings and committees as requested. Maintains clinical competence in discipline through direct patient contact as scheduled. Actively collaborates with transport staff, medical staff, and other disciplines in the development, evaluation and revision of complex patient’s plan of care in the transport environment and assists in the development of department protocols and guidelines. Assists with the development of clinical skills labs, clinical competencies, and neo/pedi transport academies and conferences as directed. Functions as clinical resource for staff and support staff as appropriate in assisting them to meet their professional goals assisting all transport disciplines to attain national certification in their area of expertise. Functions as a liaison between Transport Director, Transport Coordinators, and DCH Preceptors to determine staff support needed for successful completion of orientation and required certifications. Collaborates to evaluate the effectiveness of staff education and makes recommendations for modifications. Collaborates with clinical quality review to evaluate and assess unanticipated patient care outcomes. Education and/or Experience: Minimum of 5 years Transport Critical Care experience, with neonatal, pediatric, adult experience or combination required. A Bachelor's degree from an accredited college or university in related field is preferred Certificates, Licenses, Registrations . Current Texas license or compact state. Maintains certification in BLS, ACLS, PALS, NRP. National certification in field of discipline
RN Pediatric Full-time
Driscoll Children's Hospital

Transport RN Coordinator

apartment Driscoll Children's Hospital location_onCorpus Christi, TX
Where compassion meets innovation and technology and our employees are family. Thank you for your interest in joining our team! Please review the job information below. Transport Coordinator Through research and evidence-based practice, guides and establishes clinical best practice for the Transport Program. The Transport Clinical Coordinator serves as a key resource to medical team members on clinical matters. He/she is directly responsible to assure all training, and certifications meet or exceed standards, gathers relevant quality data to trend clinical demands, deficiencies, and develops related education and training to improve overall clinical practice. The Transport Clinical Coordinator works directly with physician medical directors, and primary receiving physicians, to measure clinical outcomes and performance improvements. He/she is cross trained in neonatal and pediatric care and meets the requirements of the Transport Coordinator duties as outlined in this job description. The Transport Clinical Coordinator reports directly to the Transport Director and works closely with peer Coordinators. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This job description is not intended to be all-inclusive; employees will perform other reasonably related business duties as assigned by the immediate supervisor and/or hospital administration as required. Maintains utmost level of confidentiality at all times. Adheres to hospital policies and procedures. Demonstrates business practices and personal actions that are ethical and adhere to corporate compliance and integrity guidelines. Identifies essential relationships and/or sees the variations in clinical patterns for Neonatal, Pediatric, and Adult patient populations. Displays intuitive grasp of patient’s status, based on broad knowledge base and expertise. Evaluates clinical practice and follows through with modifications, procedure and clinical guidelines that reflect evidence-based and research-based best practice. Participates actively in process improvement, transport education, and research activities. Complies with and integrates institutional and regulatory standard into clinical practice. Attends all transport departmental meetings and committees as requested. Maintains clinical competence in discipline through direct patient contact as scheduled. Actively collaborates with transport staff, medical staff, and other disciplines in the development, evaluation and revision of complex patient’s plan of care in the transport environment and assists in the development of department protocols and guidelines. Assists with the development of clinical skills labs, clinical competencies, and neo/pedi transport academies and conferences as directed. Functions as clinical resource for staff and support staff as appropriate in assisting them to meet their professional goals assisting all transport disciplines to attain national certification in their area of expertise. Functions as a liaison between Transport Director, Transport Coordinators, and DCH Preceptors to determine staff support needed for successful completion of orientation and required certifications. Collaborates to evaluate the effectiveness of staff education and makes recommendations for modifications. Collaborates with clinical quality review to evaluate and assess unanticipated patient care outcomes. Education and/or Experience: Minimum of 5 years Transport Critical Care experience, with neonatal, pediatric, adult experience or combination required. A Bachelor's degree from an accredited college or university in related field is preferred Certificates, Licenses, Registrations . Current Texas license or compact state. Maintains certification in BLS, ACLS, PALS, NRP. National certification in field of discipline
RN Full-time
Huntsville Hospital Health System

CLN RN Research Coordinator Heart Center Research - FT - 1st Shift

apartment Huntsville Hospital Health System location_onHuntsville, AL
Oversees and coordinates individual studies on day-to-day basis. Current Alabama Nursing Licensure Certification as Clinical Research Coordinator (CCRC) is preferred BLS Certification required within the orientation period Minimum of two years experience in Patient Care Clinical Research Coordinator experience preferred Highlights of our hospitals Huntsville Hospital was recently named Best Regional Hospital and #2 in Alabama by U.S. News & World Report . With 971 beds, a specialized Orthopedic & Spine Tower, a Level III Regional Neonatal ICU, and the largest Emergency Department and Level 1 Trauma Center in the state with our own specialized Red Shirt Trauma Program, there are many opportunities to apply your knowledge and skills. We are a certified Primary Stroke Center and named "One of the Top 100 Hospitals in the Nation with Great Heart Programs." From six cath labs and four EP labs to multiple medical and step-down units, you can continually grow your skillset! We offer a training center on campus for continuing education, Shared Governance Program, Clinical Ladder for professional development, The Daisy Award, and if you are a new grad, a Nurse Residency Program to help you transition from student to professional nurse. We care about you and your well-being by offering an excellent benefits package, childcare, health and wellness programs, an onsite employee pharmacy, a free health clinic, tuition assistance, and much more. We are committed to creating a diverse environment and proud to be an equal opportunity employer. We are a partner to the U.S. Army’s Partnership for Your Success (PaYS) program. Ask us about incentives and additional opportunities. Huntsville Hospital Benefits: We are committed to providing competitive benefits. Our benefits package for eligible employees includes medical, dental, vision, life insurance, flexible spending; short term and long term disability; several retirement account options with 401K organization match; nurse residency program; tuition assistance; student loan reimbursement; On-site training and education opportunities; Employee Discounts to phone providers, local restaurants, tickets to shows, apartment application and much more! Learn more about Huntsville Hospital Health System: Careers : https://careers.hhsys.org/careers-home Benefits : https://careers.hhsys.org/us/en/benefits Education & Professional Development : https://www.huntsvillehospital.org/education Life In Huntsville : https://www.huntsvillehospital.org/about-huntsville-al
RN Full-time
Keck Medicine of USC

Clinical Research RN Coordinator - Cardiac Research Unit - Full Time 8 Hours Day (Non-Union, Non-Exempt)

apartment Keck Medicine of USC location_onArcadia, CA
$48.41 - $76.69 / HOUR
The Clinical Research RN Coordinator position works collaboratively with investigator(s) and assists with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews. This position also addresses/resolves clinical trial patient complaints and schedules/coordinates/performs testing and/or treatments according to established protocols or as prescribed by a physician or principal investigator. Minimum Education: Bachelor’s Degree Nursing Minimum Experience: 5 years Clinical research nursing experience. Minimum Skills: Knowledge of research nursing practices, clinical expertise, and research compliance. Experience in conducting clinical research trials. Demonstrated commitment to quality service and care, teamwork, and hospital goals. Required Certifications: Registered Nurse - RN (CA Board of Registered Nursing) Basic Life Support (BLS) Provided by the American Heart Association Health Insurance Portability and Accountability Act (HIPAA) Course Certification from CITI Program Human Subjects Research (HSR) Training Certification from CITI Program Good Clinical Practice (GCP) Training Certification from CITI Program Preferred Experience: 2 years Clinical nursing experience (ICU, CCU, MICU referred) Pay Transparency The hourly rate range for this position is $48.41 - $76.69. When extending an offer of employment, the University of Southern California Arcadia Hospital considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, State, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying. We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at uschr@usc.edu . Inquiries will be treated as confidential to the extent permitted by law. Notice of Non-discrimination Employment Equity Read USC’s Clery Act Annual Security Report USC is a smoke-free environment Digital Accessibility If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser: https://wd5.myworkday.com/usc/d/inst/1$9925/9925$135151.htmld
RN Full-time
Keck Medicine of USC

Clinical Research RN Coordinator - Cardiac Research Unit - Full Time 8 Hours Day (Non-Union, Non-Exempt)

apartment Keck Medicine of USC location_onArcadia, CA
$48.41 - $76.69 / HOUR
The Clinical Research RN Coordinator position works collaboratively with investigator(s) and assists with formulating clinical research objectives, contributes to the design of clinical research protocols, oversees clinical research trials, and conducts quality assurance reviews. This position also addresses/resolves clinical trial patient complaints and schedules/coordinates/performs testing and/or treatments according to established protocols or as prescribed by a physician or principal investigator. Minimum Education: Bachelor’s Degree Nursing Minimum Experience: 5 years Clinical research nursing experience. Minimum Skills: Knowledge of research nursing practices, clinical expertise, and research compliance. Experience in conducting clinical research trials. Demonstrated commitment to quality service and care, teamwork, and hospital goals. Required Certifications: Registered Nurse - RN (CA Board of Registered Nursing) Basic Life Support (BLS) Provided by the American Heart Association Health Insurance Portability and Accountability Act (HIPAA) Course Certification from CITI Program Human Subjects Research (HSR) Training Certification from CITI Program Good Clinical Practice (GCP) Training Certification from CITI Program Preferred Experience: 2 years Clinical nursing experience (ICU, CCU, MICU referred) Pay Transparency The hourly rate range for this position is $48.41 - $76.69. When extending an offer of employment, the University of Southern California Arcadia Hospital considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate’s work experience, education/training, key skills, internal peer equity, federal, State, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. USC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by law or USC policy. USC observes affirmative action obligations consistent with state and federal law. USC will consider for employment all qualified applicants with criminal records in a manner consistent with applicable laws and regulations, including the Los Angeles County Fair Chance Ordinance for employers and the Fair Chance Initiative for Hiring Ordinance, and with due consideration for patient and student safety. Please refer to the Background Screening Policy Appendix D for specific employment screen implications for the position for which you are applying. We provide reasonable accommodations to applicants and employees with disabilities. Applicants with questions about access or requiring a reasonable accommodation for any part of the application or hiring process should contact USC Human Resources by phone at (213) 821-8100, or by email at uschr@usc.edu . Inquiries will be treated as confidential to the extent permitted by law. Notice of Non-discrimination Employment Equity Read USC’s Clery Act Annual Security Report USC is a smoke-free environment Digital Accessibility If you are a current USC employee, please apply to this USC job posting in Workday by copying and pasting this link into your browser: https://wd5.myworkday.com/usc/d/inst/1$9925/9925$135151.htmld
RN Other
MaineHealth

RN Clinical Research Nurse Coordinator - MaineHealth Institute for Research

apartment MaineHealth location_onRockport, ME
Description MaineHealth Institute for Research Nursing Req #: 55856 Summary This position is for someone interested in joining a hands-on team with the MaineHealth Coastal Region Clinical Research division of MaineHealth Institute for Research (MHIR) at MaineHealth Pen Bay Hospital, Rockport, ME and requires a valid RN license. The MaineHealth Coastal Region Clinical Research Department coordinates a wide variety of research projects at any one or more of the Coastal Region hospitals (MaineHealth Waldo Hospital, MaineHealth Pen Bay Hospital, MaineHealth Lincoln Hospital and MaineHealth Mid Coast Hospital) with the support of MHIR. These projects include industry-sponsored studies, grant-funded studies, NIH studies, as well as local investigator-initiated studies. The department works with all disciplines. Some travel between hospitals will be necessary.An onsitework schedule from ourRockport,Maine location is available for this position, with the opportunity for periodic remote chart review. The Clinical Research Nurse Coordinator may participate in any of the following, depending on the current study portfolio: Protocol development (for investigator-initiated studies) Study start-up Participant recruitment Study visit procedures (blood draws, administer surveys, etc.) Data entry Data abstraction Write-up and presentation of investigator-initiated studies Skills Needed Include Strong attention to detail Ability to maintain research integrity Willingness to learn about new indications or conditions Ability to manage several different projects at a time Self-directed Strong computer skills Clinical skills such as accurate vital signs, phlebotomy, obtaining a medical history, assessing adverse events, patient education The MaineHealth application, a cover letter and a resume or CV are all required elements for application to this position. Learn more about the MaineHealth Institute for Research in this short video. Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: Bachelor's Degree in a health science field required. Master’s Degree preferred. License/Certifications: Current applicable state license as a Registered Nurse required. Experience: Two years of clinical experience in a healthcare setting required. Additional Skills/Requirements Required: N/A Additional Skills/Requirements Preferred: N/A Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact lauren.robare@mainehealth.org
RN Full-time
Florida Cancer Specialists & Research Institute

Clinical Research Coordinator Nurse - SIGN ON BONUS

apartment Florida Cancer Specialists & Research Institute location_onFort Myers, FL
Date Posted: 2025-11-18 Country: United States of America Location: Research Fort Myers WHY JOIN FCS At Florida Cancer Specialists & Research Institute, we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training and competitive wages. Offering competitive salaries and comprehensive benefits packages to include tuition reimbursement, 401-K match, pet and legal insurance. A LITTLE BIT ABOUT FCS Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Often, FCS leads the nation in initiating research studies and offering ground-breaking new therapies to patients. Come join us today! SIGN ON BONUS - EXTERNAL CANDIDATES ONLY RESPONSIBILITIES The LPN or RN is responsible for the performance of the research study under the medical supervision of the Principal Investigator and the research director. The research coordinator is responsible for the overall successful implementation and ongoing site management of the research studies. QUALIFICATIONS LP and RN candidates must have a minimum of two years prior clinical research experience, preferably with oncology clinical research; or a minimum of three years clinical experience as an LPN, or RN in an oncology practice. Candidates must have effective communication skills, be organized, detail oriented, and strong patient advocates. Candidates must be available to travel to investigators meetings. Valid Driver’s License in state of residency for travel to clinics. Must comply with the Company Driver Safety Operations and Motor Vehicle Records Check Policy #LI-DL1 SCREENINGS – Background, drug, and nicotine screens Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized. EEOC Florida Cancer Specialists & Research Institute (FCS) is committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at FCS, please email FCS Recruitment ( Recruiter@FLCancer.com ) for further assistance. Please note this email address is intended to request an accommodation as part of the application process. Any other correspondence will not receive a response. FCS is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.
RN Full-time
Cleveland Clinic

Research Nurse Coordinator - HVTI

apartment Cleveland Clinic location_onCleveland, OH
At Cleveland Clinic Health System, we believe in a better future for healthcare. And each of us is responsible for honoring our commitment to excellence, pushing the boundaries and transforming the patient experience, every day. We all have the power to help, heal and change lives — beginning with our own. That’s the power of the Cleveland Clinic Health System team, and The Power of Every One. Job Title Research Nurse Coordinator - HVTI Location Cleveland Facility Cleveland Clinic Main Campus Department Research Administration-Research Innov and Educ Job Code T26103 Shift Days Schedule 8:00am-4:30pm Job Summary Job Details Join Cleveland Clinic’s Main Campus where research and surgery are advanced, technology is leading-edge, patient care is world class and caregivers are family. Here, you will work alongside a passionate and dedicated team, receive endless support and appreciation, and build a rewarding career with one of the most respected healthcare organizations in the world. Innovative research and groundbreaking discoveries happen every day at Cleveland Clinic. Each member of our team contributes to our mission of caring for life, analyzing health and educating caregivers. As a Research Nurse Coordinator for HVTI research, you will help us achieve this goal by overseeing the implementation and conduct of various human subject research projects. In this role, you will use your nursing knowledge to perform a variety of related tasks, including care plan development, condition evaluations, telephone triage, documentation and more. A caregiver in this role works days from 8:00 a.m. – 4:30 p.m. (start/end times flexible) After six months of orientation, there is an opportunity to work remotely one day per week. A caregiver who excels in this role will: Coordinate the implementation and conduct of research projects, ensuring adherence to research protocol requirements and timely completion. Complete and communicate regulatory documents, develop data and monitoring plans, report Serious Adverse Events as they occur, and complete FDA and sponsor forms. Serve as a liaison between investigators, research personnel, outside study personnel, and central research administration offices to assist in protocol interpretation, enrollment, and safety questions. Assess research subjects, complete nursing assessments, document findings in research subject records, and notify the physician of abnormal findings. Establish a care plan in collaboration with the research subject, family, and research team, and coordinate ongoing care. Identify discharge needs and facilitate discharge planning as appropriate. Perform telephone triage, nursing procedures, and treatments. Evaluate, initiate, and maintain standards of care consistent with CCHS policies and procedures. Assist with specialized patient care equipment as required by the clinical research protocol. Administer medications and treatments as ordered by a physician or licensed independent provider (LIP). Direct, coordinate, and participate in the evaluation and supervision of nursing care provided to research subjects, establishing patient care priorities and delegating nursing activities according to patient needs and staff capabilities. Conduct and document the informed consent process. May assist PI with research study design and development of the research protocol. May assist with research project budget development. Minimum qualifications for the ideal future caregiver include: Graduate from an accredited school of professional nursing Current state licensure as a Registered Nurse (RN) Basic Life Support (BLS) Certification through the American Heart Association (AHA) or American Red Cross Four years of clinical experience Two years of research experience Understanding of the research process and terminology In-depth knowledge of the specialty under investigation Working knowledge of federal regulations and good clinical practice (GCP) Meet clinical competency requirements Preferred qualifications for the ideal future caregiver include: Bachelor’s of Science in Nursing (BSN) Computer acumen (Outlook, Excel, research databases) Knowledge and/or experience in the OR Physical Requirements: Requires full range of body motion, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extended periods of time. Requires corrected vision and hearing to normal range. Requires working under stressful conditions and irregular hours. Exposure to communicable diseases and/or body fluids. Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Physical Demand requirements are in excess of those for Light Work. Personal Protective Equipment: Follows standard precautions using personal protective equipment as required. The policy of Cleveland Clinic Health System and its system hospitals (Cleveland Clinic Health System) is to provide equal opportunity to all of our caregivers and applicants for employment in our drug free environment. All offers of employment are followed by testing for controlled substances. Cleveland Clinic Health System administers an influenza prevention program. You will be required to comply with this program, which will include obtaining an influenza vaccination on an annual basis or obtaining an approved exemption. Decisions concerning employment, transfers and promotions are made upon the basis of the best qualified candidate without regard to color, race, religion, national origin, age, sex, sexual orientation, marital status, ancestry, status as a disabled or Vietnam era veteran or any other characteristic protected by law. Information provided on this application may be shared with any Cleveland Clinic Health System facility. Please review the Equal Employment Opportunity poster . Cleveland Clinic Health System is pleased to be an equal employment employer: Women / Minorities / Veterans / Individuals with Disabilities
RN Other
MaineHealth

RN Clinical Research Nurse Coordinator - MaineHealth Institute for Research

apartment MaineHealth location_onRockport, ME
Description MaineHealth Institute for Research Nursing Req #: 55856 Summary This position is for someone interested in joining a hands-on team with the MaineHealth Coastal Region Clinical Research division of MaineHealth Institute for Research (MHIR) at MaineHealth Pen Bay Hospital, Rockport, ME and requires a valid RN license. The MaineHealth Coastal Region Clinical Research Department coordinates a wide variety of research projects at any one or more of the Coastal Region hospitals (MaineHealth Waldo Hospital, MaineHealth Pen Bay Hospital, MaineHealth Lincoln Hospital and MaineHealth Mid Coast Hospital) with the support of MHIR. These projects include industry-sponsored studies, grant-funded studies, NIH studies, as well as local investigator-initiated studies. The department works with all disciplines. Some travel between hospitals will be necessary.An onsitework schedule from ourRockport,Maine location is available for this position, with the opportunity for periodic remote chart review. The Clinical Research Nurse Coordinator may participate in any of the following, depending on the current study portfolio: Protocol development (for investigator-initiated studies) Study start-up Participant recruitment Study visit procedures (blood draws, administer surveys, etc.) Data entry Data abstraction Write-up and presentation of investigator-initiated studies Skills Needed Include Strong attention to detail Ability to maintain research integrity Willingness to learn about new indications or conditions Ability to manage several different projects at a time Self-directed Strong computer skills Clinical skills such as accurate vital signs, phlebotomy, obtaining a medical history, assessing adverse events, patient education The MaineHealth application, a cover letter and a resume or CV are all required elements for application to this position. Learn more about the MaineHealth Institute for Research in this short video. Required Minimum Knowledge, Skills, And Abilities (KSAs) Education: Bachelor's Degree in a health science field required. Master’s Degree preferred. License/Certifications: Current applicable state license as a Registered Nurse required. Experience: Two years of clinical experience in a healthcare setting required. Additional Skills/Requirements Required: N/A Additional Skills/Requirements Preferred: N/A Additional Information With a career at any of the MaineHealth locations across Maine and New Hampshire, you’ll be working with health care professionals that truly value the people around them – both within the walls of the organization and the communities that surround it. We offer benefits that support an individual's needs for today and flexibility to plan for tomorrow – programs such as paid parental leave, a flexible work policy, student loan assistance, training and education, along with well-being resources for you and your family. MaineHealth remains focused on investing in our care team and developing an inclusive environment where you can thrive and feel supported to realize your full potential. If you’re looking to build a career in a place where people help one another deliver best-in-class care, apply today. If you have questions about this role, please contact lauren.robare@mainehealth.org Show more Show less
RN Full-time
City of Hope

RN, Post Transplant Coordinator

apartment City of Hope location_onGoodyear, AZ
RN, Post Transplant Coordinator About City of Hope , City of Hope's mission is to make hope a reality for all touched by cancer and diabetes. Founded in 1913, City of Hope has grown into one of the largest and most advanced cancer research and treatment organizations in the U.S., and one of the leading research centers for diabetes and other life-threatening illnesses. City of Hope research has been the basis for numerous breakthrough cancer medicines, as well as human synthetic insulin and monoclonal antibodies. With an independent, National Cancer Institute-designated comprehensive cancer center that is ranked top 5 in the nation for cancer care by U.S. News & World Report at its core, City of Hope’s uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas. The Cellular Therapy Post-Transplant Coordinator is a registered nurse and integral member of the Cellular Therapy team, responsible for coordinating comprehensive care for patients following Stem Cell Transplant or Immune Effector Cell (IEC) therapy (e.g. CAR-T). This role focuses on clinical monitoring, follow-up scheduling, patient and family education, resource navigation, and collaboration across inpatient, outpatient, and community settings. The coordinator supports the patient’s journey from acute care through recovery, contributing to optimal clinical outcomes, patient satisfaction, and program sustainability. The successful candidate: Must be able to work M-F 8:00a-4:30p Monitor patients for post-transplant and CAR-T therapy complications such as infections, graft-versus-host disease, and CAR-T-related toxicities. Coordinate post-transplant follow-up visits, infusion appointments, laboratory testing, and specialty referrals. Complete or submit for prior authorizations for specialty medications to avoid delays in care. Evaluate transition of care needs and arrange services across inpatient, outpatient, home health, and specialty settings. Maintain accurate and timely patient documentation in the electronic health record. Educate patients and their families about post-transplant care and self-management for better adherence to care and improved quality of life: The coordinator will provide education and support to patients and their families on topics such as managing side effects, infection prevention, and self-care after a stem cell transplant or CAR-T therapy. Reinforce discharge instructions, self-monitoring techniques, and safety precautions. Provide emotional support and counseling to patients and families navigating the post-transplant period. Connect patients to community resources, psychosocial services, survivorship programs, and support groups as appropriate. Qualifications Your qualifications should include: 3 - 5 years Oncology/Hematology Bachelor of Science in Nursing (BSN) or as approved by CAHCTI Leadership Arizona Registered Nurse License or a Registered Nurse License form a Compact State Basic Life Support (BLS) Certification Oncology Nursing Society (ONS) Chemotherapy and Biotherapy Provider Card City of Hope is an equal opportunity employer. To learn more about our comprehensive benefits, click here: Benefits Information City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.