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.