MAIN PURPOSE OF ROLE
- Experienced professional individual contributor that works under limited supervision .
- Applies subject matter knowledge in the area of Medical Affairs.
- Requires capacity to apply skills / knowledge within the context of specific needs or requirements .
MAIN RESPONSIBILITIES
- As the Experienced professional in the Medical Affairs Sub- Function , possesses well developed skills in overseeing the direction , planning , execution , clinical trials / research and the data collection activities .
- Contributes to implementation of clinical protocols , and facilitates completion of final reports .
- Recruits clinical investigators and negotiates study design and costs .
- Responsible for directing human clinical trials , phases III IV for company products under development .
- Participates in adverse event reporting and safety responsibilities monitoring .
- Coordinates and provides reporting information for reports submitted to the regulatory agencies .
- Monitors adherence to protocols and determines study completion .
- Coordinates and oversees investigator initiations and group studies .
- May participate in adverse event reporting and safety responsibilities monitoring .
- May act as consultant / liaison with other corporations when working under licensing agreements .
QUALIFICATIONS
Education
- Associates Degree ( 13 years )
Experience/Background
Role: Healthcare & Life Sciences - Other
Industry Type: Medical Devices & Equipment
Department: Healthcare & Life Sciences
Employment Type: Full Time, Permanent
Role Category: Healthcare & Life Sciences - Other
Education
UG: Any Graduate
PG: Any Postgraduate
