Indegene
Website:
indegene.com
Job details:
We are looking for a Medical Information professional with strong scientific writing expertise to support our Medical Affairs function. This role focuses on developing high-quality, evidence-based medical content and delivering accurate, balanced responses to medical queries from healthcare professionals and internal stakeholders.
This is not a call-center role—it is a scientific, content-driven position requiring deep therapeutic understanding and structured medical communication skills.
🔬 Key Responsibilities
Scientific Content Development & Review
- Develop and review standard response documents (SRDs), customized responses, FAQs, and scientific materials (e.g., infographics, slide decks)
- Ensure clear structure, logical flow, and appropriate data presentation in all deliverables
- Apply AMA style guidelines, ensuring accuracy in referencing, grammar, and scientific tone
Medical Information & Query Management
- Handle and respond to medical information enquiries from HCPs, internal stakeholders, and external audiences
- Triage enquiries involving adverse events (AEs) and product quality complaints (PQCs) to relevant teams in compliance with SOPs
- Deliver balanced, evidence-based, and non-promotional responses
Localization & Content Adaptation
- Adapt and localize global medical information content for regional requirements while ensuring compliance
Literature Review & Evidence Generation
- Conduct systematic literature searches using databases such as PubMed and Embase
- Critically evaluate and synthesize clinical data to support response development
Data Analytics & Insights
- Analyze medical inquiry data to identify trends, gaps, and insights
- Develop periodic reports and dashboards for stakeholders
Stakeholder & Project Management (Lead role)
- Lead projects end-to-end, ensuring timelines, quality, and stakeholder alignment
- Engage with cross-functional teams and clients to define content strategy and approach
- Participate in or lead client discussions, providing updates and scientific rationale
Tools & Systems
- Utilize platforms such as Veeva, IRMS, EndNote, RightFind, and Mendeley (preferred)
Quality, Compliance & Training
- Ensure adherence to quality standards, compliance policies, and confidentiality requirements
- Contribute to process improvements, documentation, and best practices
- Mentor and guide junior team members (for Lead role)
- Participate in ongoing training and capability-building initiatives
🎯 Candidate Profile
Education
- Advanced degree preferred: M.Pharm, Pharm.D, PhD, MD, BDS/MDS or relevant life sciences degree
- Candidates with strong medical writing/publication experience will also be considered
Experience
- 6–8+ years in medical information, medical writing, or medical communications
- Experience in pharmaceutical companies, biotech, or medical communications agencies preferred
Core Skills
- Proven expertise in scientific/medical writing and content development
- Strong understanding of medical information processes and compliance requirements
- Ability to interpret and communicate complex clinical data clearly and accurately
- Excellent written and verbal communication skills
- Familiarity with literature databases and referencing tools
- Basic understanding of data analysis and interpretation
🚀 What We’re Looking For
- A subject matter expert (SME) in Medical Information with a passion for scientific communication
- Strong ownership, attention to detail, and ability to work in a fast-paced, cross-functional environment
- Interest in continuous learning and staying updated with scientific advancements
❗ Important Note
We are specifically seeking candidates with content development and scientific writing experience in Medical Information in Medical Affairs. Profiles primarily focused on high-volume call handling or voice-based support roles may not be suitable for this position.
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