Job Description

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. You will be the 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 (public health, social work, sociology, psychology, communications, and more), 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 (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 Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided. 

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.

Successful candidates will possess: 

• Effective communication, good decision making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills 
• Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences 
• Prior experience in clinical trials is preferred 
• Familiarity with regulatory requirements in clinical research or ability to successfully learn this
• Experience interacting with patients and coordinating care with medical staff 
• Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol 

Education and experience requirements per tier: 

Clinical Trials Screening Coordinator: 

• Bachelor’s degree required, 2 years of experience in clinical trials (patient facing coordination, data management, regulatory or other research coordination). Knowledge of the clinical research process, procedures, and protocols.

Associate Clinical Research Coordinator: 

• Associates degree required, in lieu of Associates degree 2 years of relevant experience with a high school diploma or GED. Experience with data entry, good oral and written communication skills and organizational skills.

Clinical Research Coordinator I: 

• Bachelor's Degree with one (1) year of relevant clinical, health related, scientific, business or research experience. In lieu of a bachelor's degree, Associates degree with an additional year of relevant experience for a total of two (2) years of experience. 

Clinical Research Coordinator II: 

• Bachelor's degree with 2 years clinical trials coordination experience. In lieu of a bachelor's degree, an associate degree with 4 years of clinical trials coordination experience may be considered.

• CCRP/CCRC or equivalent preferred. 

Clinical Research Coordinator III: 

• Bachelor’s degree with 4 years of experience in clinical trials coordination. In lieu of a bachelor’s degree, associate degree with 6 years clinical trials coordination experience may be considered. 

• CCRP/CCRC certification required

Clinical Research Coordinator Sr.: 

• Bachelor's degree with 6 years of experience in clinical trial coordination. In lieu of a Bachelors' degree, associate degree with an additional 2 years of clinical trials coordination experience for a total of 8 years of experience may be considered. 
• CCRP/CCRC certification required 

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