FAQs
What is the main purpose of the Regional Medical Advisor role?
The main purpose of the Regional Medical Advisor role is to function as an experienced professional individual contributor in Medical Affairs, applying subject matter knowledge under limited supervision.
What are the primary responsibilities of the Regional Medical Advisor?
The primary responsibilities include overseeing the direction of clinical trials, implementing clinical protocols, recruiting clinical investigators, directing human clinical trials, monitoring adverse event reporting, and coordinating regulatory reporting.
What educational qualifications are required for this position?
The required educational qualification for this position is an Associates Degree, along with approximately 13 years of relevant experience.
How much experience is required for the Regional Medical Advisor position?
A minimum of 1 year of experience is required for the Regional Medical Advisor position.
Are there opportunities for involvement with clinical trials in this role?
Yes, the Regional Medical Advisor is responsible for directing human clinical trials, specifically phases III and IV for company products under development.
Will the Regional Medical Advisor need to handle safety responsibilities?
Yes, the Regional Medical Advisor will participate in adverse event reporting and safety responsibilities monitoring.
Is experience in negotiating study design and costs necessary for this position?
Yes, the role involves recruiting clinical investigators and negotiating study design and costs.
Does the role involve coordinating with other corporations?
Yes, the Regional Medical Advisor may act as a consultant/liaison with other corporations when working under licensing agreements.