Associate Director, Medical Information

Responsibilities:
- Lead scientific communication and medical information strategy for assigned therapeutic areas; ensure high-quality, compliant scientific exchange.
- Manage tactical execution of Global and US Medical Affairs medical information plans; translate insights into strategic recommendations.
- Develop and deliver scientifically accurate responses to medical inquiries, including complex issues.
- Lead creation and maintenance of medical information deliverables (e.g., literature reviews, Standard Response Documents/SRDs, verbal FAQs, Q&As, AMCP dossiers, compendium).
- Serve as medical reviewer on Promotional and Medical Review Committees to ensure medical accuracy, clarity, and compliance.
- Own department reporting processes and dashboards (metrics, insights generation, digital analytics, trend reporting).
- Evaluate, pilot, and implement AI-enabled tools to improve medical information efficiency and quality.
- Collaborate with global/regional Medical Affairs partners to align and share best practices.
- Provide scientific support for congress planning, booth activities, and real-time scientific exchange.
- Mentor/train colleagues; may directly supervise Senior Managers, Specialists, and contractors.

Qualifications:
- Minimum 5 years of Medical Information experience in the pharmaceutical industry.
- PharmD or PhD required.
- Strong therapeutic-area scientific knowledge, including evaluating and communicating clinical trial and disease state information.
- Neurology preferred.
- Demonstrated experience conducting scientific literature review and managing medical inquiries; experience developing/reviewing deliverables.
- Practical knowledge of FDA guidance.

Skills/Tools:
- Digital analytics and reporting; AI-enabled tools adoption.

Application instructions:
- Apply now.