Associate Medical Director I - Remote

Overview

The primary focus of this position is the medical review of clinical trial serious adverse events (SAEs) including causality assessment and company analysis development.

In Short

• Performs causality assessment of adverse events in post-marketing individual case safety reports.
• Performs medical review of clinical serious adverse events (SAEs).
• Develops company analysis for suspected unexpected serious adverse reactions (SUSARs).
• Responsible for accurate and timely communication with all clinical trial stakeholders.
• May serve as secondary lead for therapeutic area.
• Understands safety profile of assigned AbbVie products and development compounds.
• Understands disease state for each indication within assigned AbbVie products.
• Understands global regulations, processes and practices.
• Contributes to PSEQ initiatives and deliverables.

Requirements

• MD or DO with a minimum of 3 to 5 years of clinical experience post residency.
• Effectively analyze and guide analysis of clinical data.
• Present recommendations in group environments.
• Write, review and provide input on technical documents.
• Work collaboratively and lead cross-functional teams.
• Core competency in Microsoft Office 365 applications.

Benefits

• Comprehensive package of benefits including paid time off.
• Medical/dental/vision insurance.
• 401(k) for eligible employees.
• Eligible for short-term and long-term incentive programs.