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 Americas Best Large Employers and Americas Best Employers for Women, Computerworld magazines list of 100 Best Places to Work in Information Technology, DiversityIncs Top Hospitals & Health Systems, and continually named one of the Tampa Bay Times 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.
Additional Information
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 will bring hope to patients by delivering tomorrows 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 and smoothly, 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 are also represented. 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 a 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.
https://www.moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration
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.
Position Highlights
• Coordinate patient care by collaborating with medical staff and document in accordance with standards and regulatory guidelines with direction of a mentor or supervisor. • Act as liaison between the investigators, Moffitt regulatory staff, and the sponsor. • Assist in screening, enrolling, and following study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. • Responsible for data and source documentation and adverse experience reporting. • Perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol. • Will work under general supervision and direction from the supervisor and Principal Investigator to implement and coordinate research, including administrative procedures.
Credentials and Qualifications
• Bachelors degree preferred in a field of study, scientific health-related, or business administration program with one year of relevant clinical, health-related, scientific, business, or research experience. • In lieu of a bachelors degree, an Associates degree with two years of relevant clinical, health-related, scientific, business, or research experience.
CCRC, CCRP, CCR, or equivalent preferred.