Clinical Research Coordinator Job Tampa area,Florida USA,Healthcare

Position: CLINICAL RESEARCH COORDINATOR I

At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 is dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America’s Best Large Employers and America’s Best Employers for Women, Computerworld magazine’s list of 100 Best Places to Work in Information Technology, Diversity Inc Top Hospitals & Health Systems, and continually named one of the Tampa Bay Times’ Top Workplaces.

Additionally, Moffitt is proud to have earned the prestigious Magnet designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.

Summary

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 participating in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial.

You will be part of the team that ensures the trial progresses safely, smoothly, and according to plan.

Our Clinical Research Coordinators come from diverse backgrounds, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The role is ideal for those with healthcare experience or those seeking a new way to contribute through their careers.

This position offers a Monday through Friday schedule with hybrid work (remote and on-site) after a 90-day training period. Moffitt provides paid training and orientation through its CTO (Clinical Trials Office) Academy. Position tiers vary based on experience, and relocation assistance may be available.

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This role involves working closely with patients, families, study sponsors (from biotech startups to large pharmaceutical companies), and the Clinical Trial Team, including physicians, pharmacists, nurses, data monitors, and data managers.

Position Highlights:

Coordinate patient care by collaborating with medical staff and documenting in accordance with standards and regulatory guidelines, under supervision.

Act as a liaison between investigators, Moffitt regulatory staff, and sponsors.

Assist in screening, enrolling, and monitoring study subjects, ensuring protocol compliance and safety.

Handle data and source documentation, and report adverse experiences.

Perform administrative duties requiring analysis, sound judgment, and knowledge of study protocols.

Work under supervision to implement and coordinate research activities, including administrative procedures.

Credentials and Qualifications:

Bachelor’s degree in a scientific, health-related, or business administration field preferred, with one (1) year of relevant experience.
Alternatively, an Associate’s degree with two (2) years of relevant experience.
CCRP/CCRC or equivalent certification is preferred.

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