Regional Medical Advisor

<p><b>MAIN PURPOSE OF ROLE</b></p><p></p><p>Experienced professional individual contributor that works under limited supervision.</p><p>Applies subject matter knowledge in the area of Medical Affairs.</p><p>Requires capacity to apply skills/knowledge within the context of specific needs or requirements.</p><p><span> </span></p><p><b>MAIN RESPONSIBILITIES</b></p><p></p><p>

• 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.</p><p>
• Contributes to implementation of clinical protocols, and facilitates completion of final reports.</p><p>
• Recruits clinical investigators and negotiates study design and costs.</p><p>
• Responsible for directing human clinical trials, phases III & IV for company products under development.</p><p>
• Participates in adverse event reporting and safety responsibilities monitoring.</p><p>
• Coordinates and provides reporting information for reports submitted to the regulatory agencies.</p><p>
• Monitors adherence to protocols and determines study completion.</p><p>
• Coordinates and oversees investigator initiations and group studies.</p><p>
• May participate in adverse event reporting and safety responsibilities monitoring.</p><p>
• May act as consultant/liaison with other corporations when working under licensing agreements.</p><p></p><p><b>QUALIFICATIONS</b></p><p></p><p><b>Education</b></p><p>Education Level : Associates Degree (± 13 years) </p><p><span> </span></p><p><b>Experience/Background</b></p><p>Experience : Minimum 1 year</p>