Clinical Research Coordinator

Apply for the CLINICAL RESEARCH COORDINATOR I position at Moffitt Cancer Center
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Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial.

You will be a member of the team that ensures the trial is moving forward safely, smoothly, and according to plan.

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

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

Entry level

Full‑time

Research, Analyst, and Information Technology

Hospitals and Health Care