Clinical Research Coordinator

CLINICAL RESEARCH COORDINATOR I

Join Moffitt Cancer Center as a Clinical Research Coordinator to impact lives by delivering innovative cancer treatments through clinical trials.

As a Clinical Research Coordinator, you will interact directly with patients, enrolling and guiding them through therapeutic clinical trials, while ensuring the trial progresses safely, smoothly, and in accordance with protocol. The role welcomes a range of backgrounds—including social sciences, biological sciences, business, and humanities—and offers a Monday–Friday schedule with hybrid work after a 90‑day training period.

• Coordinate patient care, collaborating with medical staff and documenting in accordance with regulatory guidelines with direction of a mentor or supervisor.
• Act as liaison between investigators, Moffitt regulatory staff, and sponsors.
• Assist in screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring while on study.
• Responsible for data and source documentation and adverse event reporting.
• Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
• Work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.

• Bachelor’s degree (preferred scientific, health‑related, or business administration) with one year of relevant clinical, health‑related, scientific, business, or research experience.
• In lieu of a bachelor’s degree, Associate’s degree with two years of relevant experience.
• CCRP/CCRC or equivalent preferred.