Regional Medical Advisor

MAIN PURPOSE OF 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

u2022 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.

u2022 Contributes to implementation of clinical protocols, and facilitates completion of final reports.

u2022 Recruits clinical investigators and negotiates study design and costs.

u2022 Responsible for directing human clinical trials, phases III & IV for company products under

development.

u2022 Participates in adverse event reporting and safety responsibilities monitoring.

u2022 Coordinates and provides reporting information for reports submitted to the regulatory agencies.

u2022 Monitors adherence to protocols and determines study completion.

Coordinates and oversees investigator initiations and group studies.

u2022 May participate in adverse event reporting and safety responsibilities monitoring.

u2022 May act as consultant/liaison with other corporations when working under licensing agreements.

QUALIFICATIONS

Education

Education Level Major/Field of Study or Equivalent

Associates Degree (u00B1 13

years)

Experience/Background

Experience Experience Details

Minimum 1 year