Medical Information Lead – Medical Affairs Full Time NEW

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.