Work as Medical Information Manager at Indegene

We help biopharmaceutical, emerging biotech and medical device companies develop products, get them to the market, and grow their impact through the life cycle in a more effective, efficient, and modern way. We bring together healthcare domain expertise, fit-for-purpose technology, and an agile operating model to provide a diverse range of solutions. These aim to deliver, amongst other outcomes, a personalized, scalable and omnichannel experience for patients and physicians. It’s what drives our team and our purpose to enable healthcare organizations to be future ready.

Post : Medical Information Manager

Job Description
We are seeking a highly motivated and experienced professional to serve as a Medical Information (MedInfo) Manager for multiple brands & therapeutic areas of a leading global pharmaceutical company. This individual will be responsible for developing and driving the content roadmap aligned with the evolving needs of a dynamic portfolio—balancing loss of exclusivity (LoE) scenarios with upcoming launches The ideal candidate will serve as the single point of contact between the client and the vendor team(s), leading prioritization, innovation, and governance of medical information content in a complex, fast-paced environment.

Key Responsibilities :
• Content Planning & Prioritizatio
• Develop and maintain a content roadmap for MedInfo assets across multiple brands and therapeutic areas
• Prioritize content development activities based on document expiry, product lifecycle, market needs, and internal stakeholder input.
• Content Optimization
• Audit existing medical information letters and recommend retirements, consolidations, or updates.
• Drive content lifecycle management in alignment with compliance, regulatory, and scientific standards.
• Innovation in Content Formats & Topics
• Identify opportunities for new content formats (e.g., modular, interactive, or digital formats) to improve 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 the vendor team(s).
• Facilitate seamless communication, status tracking, and delivery of high-quality content assets.
• Process & Platform Expertise
• Ensure strategic alignment with internal SOPs, processes, and quality standards.
• Leverage knowledge of Veeva Vault (MedComms/PromoMats) to manage content workflows and metadata efficiently.

Candidate Profile
• 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 medical affairs content roles
• Strong understanding of product lifecycle management, especially LoE and launch planning
• Good understanding of the end-to-end lifecycle of standard response documents/medical information letters, with preferred experience in both writing and reviewing such documents
• Robust understanding of the US regulatory landscape for Medical Information, including compliance considerations for content creation and disseminationExperience with
• Veeva Vault (mandatory)
• Excellent communication, cross-functional collaboration, and project management skills
• Prior experience working with US-based clients and coordination with vendors across various time zones is a plus

Key Competencies :
• Strategic thinking and content planning
• Scientific acumen
• Process orientation and compliance awareness
• Strong interpersonal and stakeholder management skills
• Flexibility to adapt to evolving portfolio needs

Additional Information
Experience : 3-5 years
Qualification : Advanced degree in Life Sciences, Pharmacy
Location : NJ, US
Industry Type : Pharma/ Healthcare/ Clinical research
End Date : 10th July 2025