CLINICAL RESEARCH COORDINATOR II

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 are 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, DiversityInc Top Hospitals & Health Systems, and continually named one of the Tampa Bay Time’s Top Workplace. 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 a 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), biological sciences, business, and humanities. This role is ideal for those with healthcare experience or those seeking a new way to contribute through their career. 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. Relocation assistance may be available. https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration This role involves close collaboration with patients, their families, study sponsors, and the Clinical Trial Team, including physicians, pharmacists, nurses, data monitors, and data managers. Position Highlights: Supports the Principal Investigator (PI) in clinical trials by implementing and coordinating research activities at Moffitt Cancer Center. Acts as the primary resource for protocols, coordinating patient care with medical staff, and documenting in accordance with standards and regulatory guidelines. Serves as a liaison between investigators, care providers, regulatory staff, and sponsors. Screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring during the study. Performs core support for clinical research coordination and manages more complex studies with higher patient volumes. Determines methods and procedures for the coordination of newly assigned studies. Credentials and Qualifications: Bachelor’s degree with 2 years of clinical trials coordination experience; or Associate’s degree with 4 years of clinical trials coordination experience (considered in lieu of a bachelor’s degree) CCRP/CCRC certification preferred.

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