RESEARCH DATA COORDINATOR I

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. Responsibilities Interact directly with patients, enrolling, educating and guiding them through clinical trials. Collaborate with patients’ families, study sponsors and the Clinical Trial Team (physicians, pharmacists, nurses, data monitors and data managers). Ensure the trial progresses safely, smoothly, and according to plan. Support data management tasks: review and synthesize information from medical records, enter data into study databases, and resolve data queries. Work with the study coordinator and monitors to ensure all data requirements are met and captured per protocol. Qualifications Effective communication, good decision‑making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and strong time‑management skills. Excellent teamwork skills and ability to collaborate with those from diverse backgrounds. Prior experience in clinical trials is preferred. Familiarity with regulatory requirements in clinical research or a demonstrated ability to learn quickly. Experience interacting with patients and coordinating care with medical staff. Benefits & Expectations The position offers a Monday through Friday schedule and a hybrid work model (remote and on‑site) after a 90‑day introductory and training period. Moffitt provides paid training and orientation through its Clinical Trials Office Academy. Position tiers may vary with experience, and relocation assistance may be provided. #J-18808-Ljbffr Moffitt Cancer Center