Regional Medical Advisor

Role Overview: You will work as an experienced professional individual contributor in the area of Medical Affairs with limited supervision. Your role will involve applying subject matter knowledge to meet specific needs or requirements. Key Responsibilities: - Possess well-developed skills in overseeing direction, planning, execution, clinical trials/research, and data collection activities in the Medical Affairs Sub-Function. - Contribute to the implementation of clinical protocols and facilitate the completion of final reports. - Recruit clinical investigators, negotiate study design and costs. - Direct human clinical trials, phases III & IV for company products under development. - Participate in adverse event reporting and safety responsibilities monitoring. - Coordinate and provide reporting information for reports submitted to regulatory agencies. - Monitor adherence to protocols and determine study completion. - Coordinate and oversee investigator initiations and group studies. - Act as a consultant/liaison with other corporations when working under licensing agreements. Qualifications: - Associates Degree (13 years) - Minimum 1 year experience,