DIR CLINICAL TRIALS OPERATIONS

DIR CLINICAL TRIALS OPERATIONS

Tampa, FL Job Details Full-time 1 hour ago Qualifications Clinical research Operations management 5 years Bachelor's degree in business Research Project management Clinical research compliance Financial operations management Bachelor's degree Team management Quality improvement Research administration Healthcare financial management Research regulatory compliance Productivity software Senior level Strategic partnerships Business Leadership Communication skills Technical Proficiency Full Job Description Tampa, FL Moffitt at Magnolia Campus (MCC)

CTO OPERATIONS 2

Full Time - Day Shift - M-F Req #: 93421 Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 10,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time's Top Workplaces. A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001.

Summary Job Summary:

The Director Clinical Trials Operations is responsible for the development, implementation and leadership of personnel, infrastructure, and financial management for one or more Clinical Trial Area in a compliant, effective, and efficient manner. It provides leadership and strategic partnership to physician leadership in trial portfolio and pipeline management, which includes relationships with trial sponsors (Pharm and Biotech Companies). The position leads problem solving and improvement efforts, including the incorporation of new technology and approaches that improve quality and performance in clinical trials operations.

Minimum Experience Required:

Bachelor's Degree Medical/Scientific or Business Eight (8) years of progressive experience and responsibility in executing multidisciplinary clinical research, inclusive of five (5) years management/leadership experience in a clinical research/academic setting. Ability to apply knowledge of regulations that govern clinical research. Knowledge of NCI designated cancer centers or equivalent large specialized academic institutions. Current knowledge of best practices in clinical research, including active participation in national organizations, such as the AACI CRI, SOCRA, or ACRP. Proficient business software skills including Microsoft Office. Proficient with clinical trials management systems (CTMS). Demonstrated well-developed project management and problem-solving skills. Demonstrated experience in personnel management and professional development. Strong interpersonal and communication skills (written and oral).