What are the responsibilities and job description for the SPVR CLINICAL TRIALS OFFICE position at Moffitt Cancer Center Careers?
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
Position Highlights:
- Provides basic day-to-day supervision of the clinical research staff and operations assigned with oversight from responsible CTO manager and in collaboration with faculty and investigators.
- Works effectively across the organization and externally with sponsor organizations to ensure effective and efficient conduct of clinical research.
- Supports the recruiting, training, development, and performance management of assigned staff.
- Operationally focuses on study start up, trial coordination, and quality assurance needs, providing problem-solving and troubleshooting expertise.
- Will be expected to identify process improvement opportunities, collaborate with their team to develop creative solutions, lead/delegate implementation, and track success through defined metrics.
Responsibilities:
- Provide daily supervision of research staff including scheduling to meet program business needs and orientation and training.
- Supervise the staff responsibilities for the clinical aspects of study start up.
- Serve as resource to investigators writing investigator-initiated trials.
- Perform quality assurance procedures to check work of assigned staff for accuracy and completeness.
- Work with the CTO manager to improve organizational performance through recommending areas or approaches for improvement activities, performing new procedures, collecting data and providing input to department discussions.
Credentials and Qualifications:
- Bachelor's degree.
- (Science or Health care related field preferred; Masters preferred)
- SoCRA or ACRP (or equivalent) certification.
- Four (4) years experience in clinical trials (patient facing coordination, data management, regulatory, or other research coordination).
- Oncology trials knowledge, OnCore CTMS experience preferred.
- Supervisory, or team lead experience preferred