Clinical Research Coordinator I - Breast
About The Position
Moffitt Cancer Center is hiring a Clinical Research Coordinator to help coordinate therapeutic cancer clinical trials. The role works directly with patients, enrolling, educating, and guiding them through trial participation while helping ensure studies proceed safely, smoothly, and according to protocol. Coordinators collaborate with patients and their families, study sponsors, and a clinical trial team that includes physicians, pharmacists, nurses, data monitors, and data managers. The coordinator works under general supervision and with direction from a supervisor, mentor, or Principal Investigator to implement and coordinate research and related administrative procedures. The position offers a Monday-through-Friday schedule and a hybrid work arrangement, combining remote and on-site work after completion of a 90-day introductory and training period. Paid training and orientation are provided through Moffitt’s Clinical Trials Office Academy. Position tier may vary according to experience, and relocation assistance may be provided.
Requirements
- Bachelor’s degree, preferably in a scientific, health-related, or business administration field, and one year of relevant clinical, health-related, scientific, business, or research experience; alternatively, an associate degree and two years of relevant experience.
Nice To Haves
- CCRP, CCRC, or equivalent certification.
Responsibilities
- Coordinate patient care in collaboration with medical staff and document in accordance with standards and regulatory guidelines, with direction from a mentor or supervisor.
- Act as a liaison among investigators, Moffitt regulatory staff, and study sponsors.
- Assist with screening, enrolling, and following study subjects.
- Ensure protocol compliance and closely monitor subjects while they are on study.
- Manage data and source documentation and report adverse experiences.
- Perform diverse administrative duties requiring analysis, sound judgment, and thorough knowledge of the study protocol.
- Implement and coordinate research, including administrative procedures, under the general supervision and direction of the supervisor and Principal Investigator.
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
Entry Level
