Clinical Research Coordinator II
About The Position
The Clinical Research Coordinator II supports the Principal Investigator in implementing and coordinating clinical trials, including related administrative procedures at Moffitt Cancer Center. As the primary resource for study protocols, the coordinator works with medical staff to coordinate patient care and document activities in accordance with standards and regulatory guidelines. The role serves as a liaison among investigators, care providers, Moffitt regulatory staff, and study sponsors. In collaboration with the investigator, the coordinator screens, enrolls, and follows study subjects, ensuring protocol compliance and close monitoring while participants are on study. The CRC II performs core Clinical Research Coordinator support duties and takes on additional responsibilities for more complex studies with higher patient volume. The position also determines methods and procedures for coordinating newly assigned studies. The role involves interaction with patients and their families, study sponsors, and clinical trial team members such as physicians, pharmacists, nurses, data monitors, and data managers. The schedule is Monday through Friday. Hybrid work, combining remote and on-site work, is available after completing a 90-day introductory and training period. Paid training and orientation are provided through the Clinical Trials Office Academy. Position tiers may vary by experience; relocation assistance may be provided.
Requirements
- Bachelor’s degree and 2 years of clinical trials coordination experience; alternatively, an associate’s degree and 4 years of clinical trials coordination experience may be considered.
Nice To Haves
- CCRP or CCRC certification is preferred.
Responsibilities
- Support the Principal Investigator in implementing and coordinating clinical trials, including administrative procedures.
- Serve as the primary protocol resource and coordinate patient care in collaboration with medical staff.
- Document study activities in accordance with standards and regulatory guidelines.
- Liaise among investigators, care providers, Moffitt regulatory staff, and study sponsors.
- Screen, enroll, and follow study subjects in collaboration with the investigator.
- Ensure protocol compliance and closely monitor subjects while they are on study.
- Perform core Clinical Research Coordinator support duties and additional responsibilities for complex studies with higher patient volume.
- Determine methods and procedures for coordinating newly assigned studies.
Benefits
- Paid training and orientation through the Clinical Trials Office Academy.
- Relocation assistance may be provided.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
