Donor Research Coordinator, Sr. jobs in Tampa, FL

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

Job Summary:

The Clinical Research Coordinator Sr. (CRC Sr.) is the most senior level in the CRC career path, with mentoring and training responsibilities for the team or department within Clinical Trials, at Moffitt Cancer Center. The CRC Sr. works independently and maintains the highest level of expertise including administrative procedures.
 

The CRC Sr. is required to be highly proficient regarding determining methods and procedures on new protocol requirements while implementing good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the CRC Sr will coordinate complex protocol required patient care procedures by collaborating with medical staff, and document in accordance with standards and regulatory guidelines. Along with the investigator, the CRC Sr will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. The CRC Sr will perform all CRC core support and additional responsibilities as detailed for CRC III with the expectation of ability to carry a higher study/patient work-load and assist lower level coordinators with their work-load. In addition, the CRC Sr is expected to contribute significantly to the education, mentorship, process
development, and quality improvement of the team and department.
 

The CRC, Sr. works under minimal supervision with wide latitude for independent judgment. Determines methods and procedures on new assignments. May be asked to lead meetings or act as a project lead for team or other role based initiatives. Works on complex issues where analysis of situations or data requires in-depth evaluation of variable factors. Exercise judgment in selecting methods, techniques and evaluation criteria for obtaining results. Networks with key contacts outside own area of expertise. Requires specialized depth and/or breadth of expertise in own field. Guides others in resolving complex issues in specialized area based on existing solutions and procedures. Serves as best practical/quality resource within own discipline or as a technical expert on functional or cross-functional teams or projects. Trains/mentors.

Minimum Experience Required: 

Bachelor's degree with six (6) years of experience in clinical trial coordination. In lieu of a Bachelors' degree, Associate's degree with an additional two years of clinical trials coordination experience for a total of eight (8) years of experience may be considered.

CCRP/CCRC or equivalent required. 

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’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. 

https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ 

Clinical Trials 

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