Abbott - Senior Medical Advisor

MAIN PURPOSE OF ROLE

Summarize the main purpose of the role:

- Specialist professional individual contributor with comprehensive knowledge in the area of Medical Affairs.

- Ability to execute highly complex or specialized projects.

- Adapts precedent and may make significant departures from traditional approaches to develop solutions.

Main Responsibilities

- As the Specialist in the Medical Affairs Sub-Function, considered as highly experienced and knowledgeable resource within the organization 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

Education: MD Pharmacology (Mandatory)

Experience - 2 - 5years