The Associate Medical Director will work out of Abbott global headquarters in Abbott Park, IL. For the right candidate, we are offering a full relocation package.

This Associate Medical Director will be responsible for the following:

Provide medical review of safety protocols, and clinical brochures.

Serve as sub-investigator or primary investigator for Clinical Pharmacology and Phase 1 clinical studies.

Monitor and summarize clinical adverse events; maintain all aspects of medical safety for product lines.

Evaluate safety data involving INDs/NDAs and provide interim and final analyzing of reports for such projects.

Maintain liaisons with, and provide evidence based advice to Quality Assurance, Document Management, Clinical teams, Legal, and Regulatory Affairs.

Manage and mentor clinical research team members as required by assigned projects.

QUALIFICATIONS:

Basic Qualifications:
This individual should have a minimum of 1 year of clinical experience within a pharmaceutical company, private practice, academic, or CRO setting, especially as related to clinical pharmacology or early phase clinical development.

A strong familiarity with the FDA, and experience with FDA inquiries involving drug safety and efficacy including the ability to review safety and labeling protocols, are essential.

Other attributes include: administrative ability; strong interpersonal and leadership skills, self-motivation, and high personal integrity and ethics required.

The qualified candidate will be a physician with U.S. board certification in Internal Medicine, Emergency Medicine or Family Medicine, and active US license that is transferable to State of Illinois within 3 months.

Preferred Qualifications:
The ideal candidate will have clinical research experience within a pharmaceutical or CRO clinical pharmacology setting.
He or she will also have experience working in project oriented cross-functional and matrix teams.

If interested, please apply online at http://track.jobviper.com/ViewJob.asp?id=630978-1281-3169