The Ohio State University is looking to solve the problem of managing and overseeing the conduct of clinical trials of a cancer disease-specific research team within OSUCCC Clinical Trials Office (CTO).
Requirements
- Knowledge of clinical research regulations, guidelines & compliance issues required including Institutional Review Board (IRB) & federal or industry sponsor processes and requirements
- ACRP (Assn of Clinical Research Professionals) or SOCRA (Society of Clinical Research Associates) certification required
- Knowledge of clinical trials data management preferred
- Experience in a clinical research capacity conducting & implementing research projects required
- Experience in a progressively responsible administrative or management research capacity preferred
- Supervisory experience preferred
- Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required
Responsibilities
- Oversees planning, organization, implementation, and execution of all clinical research projects specific to disease team
- Manages and supervises daily administrative, operational, research and patient care activities in a specific cancer disease site collaborating and communicating with faculty, administration, research staff and shared resources within James Cancer Hospital and OSUCCC as appropriate
- Plans, directs, assigns, and monitors team workflow, activities, and productivity to ensure fulfillment of research goals
- Develops and implements plans to meet requirements of new studies/protocols and ensures all requirements within disease team are met; plans and leads disease team meetings at which protocol activity and progress, resource allocations and productivity benchmarks are reviewed
- Conducts quality assurance reviews of research processes and data
- Collaborates with OSUCCC investigators and regulatory staff in the development, review, submission, and implementation of research protocols
- Manages and supervises recruitment, interviews, screening and enrolling of patients into research protocols
Other
- 5 yrs. experience in a clinical research capacity conducting & implementing research projects required
- Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required
- Final candidates are subject to successful completion of a background check
- A drug screen or physical may be required during the post offer process
- The university is an equal opportunity employer, including veterans and disability
