PV Specialist

As an experienced professional individual contributor in the Medical Affairs Sub-Function, you will work under limited supervision and apply subject matter knowledge in the field of Medical Affairs. You should have the capacity to apply your skills and knowledge within the context of specific needs or requirements. Your main responsibilities will include: - Overseeing the direction, planning, execution, clinical trials/research, and data collection activities in the Medical Affairs Sub-Function. - Contributing to the implementation of clinical protocols and facilitating the completion of final reports. - Recruiting clinical investigators, negotiating study design and costs, and directing human clinical trials, phases III & IV for company products under development. - Participating in adverse event reporting and safety responsibilities monitoring. - Coordinating and providing reporting information for reports submitted to regulatory agencies. - Monitoring adherence to protocols and determining study completion. - Coordinating and overseeing investigator initiations and group studies. - Acting as a consultant/liaison with other corporations when working under licensing agreements. No additional details of the company are mentioned in the Job Description.,