Posted:3 months ago| Platform:
Work from Office
Full Time
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 Minimum 1 year
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