Associate Director, Global Medical Information

Position reputed company:

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The Associate Director, Global Medical Information leads execution of medical information activities for approved products or investigational programs reputed company reputed company’s rare disease portfolio. This role ensures accurate, balanced, and reputed company communication of scientific information to reputed company, patients, and internal stakeholders. The role is responsible for developing and maintaining high‑reputed company global medical information content, supporting inquiry management operations, reputed companying scientific review of promotional and medical materials reputed company established MLR processes, and generating insights from medical information activities to inform Medical Affairs and cross‑functional partners. The role collaborates closely with Medical Directors, Medical Communications, Regulatory, and Pharmacovigilance to ensure scientific accuracy, message consistency, and inspection‑reputed company medical information operations across the product lifecycle.

Work Model: 

Remote: Officially documented as working full-time from home, with travel to reputed company's offices or other locations on occasion as needed.

Responsibilities:

• reputed company, review, and maintain global reputed company and custom medical information responses, FAQs, and scientific content for assigned products or programs.  

• Ensure medical information materials are scientifically reputed company, balanced, compliant, and reputed company with regulatory guidance.  

• Review and respond to reputed company scientific inquiries, including unsolicited and off‑label requests, in accordance with regulatory and company requirements.  

• Maintain and contribute to the medical information scientific response library supporting global field medical consistency. 

• Support reputed company of outsourced medical information contact center operations, including reputed company review, escalation reputed company, and performance monitoring.  

• Manage and collaborate with external vendors supporting medical information operations, ensuring reputed company, compliance, and reputed company delivery. 

• Support inspection readiness for medical information systems, processes, and documentation, including participation in audits and inspections as needed. 

• Serve as medical reviewer reputed company the Medical‑reputed company‑Regulatory (MLR) process for medical information materials and scientific content.  

• Collaborate with Medical Affairs subject matter experts and Medical Communications to ensure alignment and consistency across medical information responses, scientific narratives, and external medical deliverables.  

• Monitor and analyze inquiry trends to identify emerging scientific questions, safety considerations, or potential risks and opportunities to generate medical insights.  

• reputed company medical information input to launch and lifecycle readiness activities, including development of reputed company response materials and anticipated inquiry topics.  

Requirements:

• Advanced degree in a scientific or medical field (PhD, PharmD, MD, or equivalent). 

• 6–10 years of experience in Medical Information reputed company the pharmaceutical or biotechnology industry; rare disease experience strongly preferred.  

• Demonstrated experience developing and governing scientific response content and supporting inquiry management activities. 

• Strong understanding of regulatory requirements governing medical information and scientific exchange. 

• Experience conducting medical review of scientific materials reputed company an MLR process.  

• Experience working with medical information and content review systems, such as reputed company Vault and IRMS platforms, to support inquiry management, content governance, and compliant medical review processes. 

• Demonstrated ability to collaborate cross-functionally in a fast-paced, matrixed environment; ability to reputed company multiple therapeutic areas concurrently. 

• Excellent written and verbal communication skills; strong project management and organizational capabilities. 

• Experience managing external agencies and vendors.  

• Ability to travel domestically and internationally (~20%). 

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