Main Responsibilities
- Oversee direction, planning, execution, clinical trials/research, and data collection activities in Medical Affairs Sub-Function.
- Implement clinical protocols and facilitate completion of final reports.
- Recruit clinical investigators and negotiate study design and costs.
- Direct human clinical trials, phases III & IV for company products under development.
- Participate in adverse event reporting and safety monitoring.
- Coordinate and provide reporting information for regulatory agency submissions.
- Monitor adherence to protocols and determine study completion.
- Coordinate and oversee investigator initiations and group studies.
- Act as consultant/liaison with other corporations under licensing agreements.
Qualifications
Education: Associate’s Degree (± 13 years) in a related field.
Experience: Minimum 1 year in Medical Affairs or related background.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Health Care Provider
Industry
Hospitals and Health Care