Medical Information Lead
Location: New Jersey, United States
Date Posted: April 29, 2025
About the Role:
Indegene is seeking a Medical Information (MedInfo) Lead to manage content development and lifecycle for multiple therapeutic areas and brands of a global pharmaceutical leader. In this role, you will be responsible for developing and driving a content roadmap that aligns with market needs, regulatory requirements, and product lifecycle management. The MedInfo Lead will serve as the primary point of contact between client stakeholders and vendor teams, ensuring high-quality content delivery in a fast-paced, complex environment.
Key Responsibilities:
Content Planning & Prioritization:
Develop and maintain a content roadmap for MedInfo assets across multiple brands and therapeutic areas.
Prioritize content development based on factors like document expiry, product lifecycle, and market needs.
Content Optimization:
Audit and optimize existing medical information letters, recommending updates, retirements, or consolidations.
Manage content lifecycle in alignment with compliance, regulatory, and scientific standards.
Innovation in Content Formats & Topics:
Explore opportunities for new content formats (modular, interactive, digital) to enhance HCP engagement.
Propose new topics that align with evolving medical trends, product needs, and customer queries.
Stakeholder Liaison & Project Leadership:
Act as the single point of contact between client stakeholders (Medical Affairs, Regulatory, Legal, Compliance) and vendor teams.
Ensure seamless communication, status tracking, and timely delivery of high-quality content.
Process & Platform Expertise:
Ensure strategic alignment with internal SOPs, processes, and quality standards.
Utilize Veeva Vault (MedComms/PromoMats) to manage content workflows and metadata efficiently.
Required Qualifications:
Advanced degree in Life Sciences, Pharmacy, or a related field (PharmD, PhD, MD, or MS preferred).
3-5 years of experience in Medical Information, Scientific Communications, or related roles in medical affairs content.
Strong understanding of product lifecycle management, particularly loss of exclusivity (LoE) and launch planning.
Knowledge of the full lifecycle of medical information documents, with experience in both writing and reviewing them.
Expertise in the US regulatory landscape for Medical Information and compliance considerations.
Experience with Veeva Vault is mandatory.
Excellent communication, cross-functional collaboration, and project management skills.
Prior experience working with US-based clients and vendors across multiple time zones is a plus.
Key Competencies:
Strategic thinking and content planning.
Strong scientific acumen.
Process orientation and compliance awareness.
Excellent interpersonal and stakeholder management skills.
Ability to adapt to evolving portfolio needs.
Equal Opportunity Statement:
Indegene is committed to a culture of inclusion and diversity. We do not discriminate based on race, religion, sex, age, national origin, gender identity, sexual orientation, disability, or any other characteristic. All employment decisions will be made based on business needs and candidate qualifications.
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