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.
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.

Summary

The Clinical Trials Resource Pool in the Clinical Trials Office is looking for a Clinical Trials Coordinator I.  

Position Highlights:

Will serve as the centralized point of contact for communication regarding clinical trials in the start-up process. Facilitates the execution of opening clinical trials to accrual within the designated program patient population. Communicates protocol specific information to primary clinical trial coordinator and principle investigator during the start-up phase of the protocol. Will work with general guidance from supervisor to implement clinical trials through pre-site selection, SRC review, IRB approval, collaboration with ancillary departments, creation of protocol orders and other source documentations and finally SIV and protocol activation.

Ideal Candidate:

Will have in-depth knowledge of good clinical practices as set forth by Federal regulations. Previous coordinator experience, oncology background preferred. Engaged, organized individual with strong critical thinking skills who has the ability to work efficiently under pressure. Highly motivated, shows initiative, is proactive and able to work independently as well as in a team.

Responsibilities:

Coordinate clinical research protocols throughout the start-up phase of the trial Work collaboratively with specific departments to help maintain appropriate documents. Verify the accuracy and completion of documentation including but not limited to, subject eligibility checklist, source documentations, drug dispensing logs, subject screening logs, and study-related communication.  Will interact directly with patients, study sponsors, managers and other department personnel.

Credentials and Qualifications:

Minimum high school diploma with eight (8) years of relevant clinical research experience required OR Associates degree with four (4) years of relevant clinical research experience required.   Bachelor's degree preferred