Research Data Coordinator

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 the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial.

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

Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.

This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90‑day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trials Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided.

(Use the "Apply for this Job" box below)./

These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.

• Effective communication, good decision‑making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences
• Prior experience in clinical trials is preferred
• Familiarity with regulatory requirements in clinical research or ability to learn these successfully
• Experience interacting with patients and coordinating care with medical staff

Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol.

High School Diploma/GED with 1 year experience using automated data processing techniques, word processing software or database software programs.

• In lieu of experience, an AA/AS degree is acceptable.