Clinical Research Coordinator I
3 days ago
Moffitt Cancer Center is a leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our team of over 9,000 is dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. We have 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.
We are 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.
As a Clinical Research Coordinator, you will bring hope to patients by delivering tomorrow's cancer treatments today. You will 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 a 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, 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 after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO Academy. Position tiers may vary according to experience. Relocation assistance may be provided.
As a Clinical Research Coordinator, you will work closely with patients, patient families, study sponsors, and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors, and data managers. Your responsibilities will include coordinating patient care, acting as a liaison between investigators, regulatory staff, and sponsors, assisting with screening, enrolling, and following study subjects, and performing administrative duties requiring analysis, sound judgment, and a high level of knowledge of study protocol.
We are an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, or protected veteran or disabled status. We seek candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence.
Reasonable accommodation will be provided to qualified individuals with disabilities. Please inform us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.
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