Description

<h2>JOB DESCRIPTION:</h2>MAIN PURPOSE OF THE 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 Associates Degree (± 13 years) Minimum 1 year experience     The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted. <h2>JOB FAMILY:</h2>Medical & Scientific Affairs     <h2>DIVISION:</h2>EPD Established Pharma        <h2>LOCATION:</h2>India > Mumbai : BKC Building     <h2>ADDITIONAL LOCATIONS:</h2>     <h2>WORK SHIFT:</h2>Standard     <h2>TRAVEL:</h2>Not specified     <h2>MEDICAL SURVEILLANCE:</h2>Not Applicable     <h2>SIGNIFICANT WORK ACTIVITIES:</h2>Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Medical Advisor

Description

Abbott

Pipeline