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Medical Information Manager

TCS
4-8 years
INR 10 LPA – 20 LPA
Bangalore, Hyderabad, Mumbai, India
1 June 15, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model

Medical Information Manager

Location: Mumbai, Hyderabad, Bengaluru, Noida, India
Employment Type: Full-Time

Job Summary

The Medical Information Manager is responsible for developing, reviewing, and maintaining scientifically accurate, evidence-based medical information content to support healthcare professionals, patients, and internal stakeholders. This role involves conducting comprehensive literature reviews, preparing medical enquiry responses, managing scientific communications, and ensuring compliance with regulatory, medical, and company standards.


Key Responsibilities

Medical Information & Scientific Response Development

  • Develop, review, and maintain high-quality medical information content and response documents.

  • Author scientifically balanced, evidence-based responses to medical enquiries from healthcare professionals and other stakeholders.

  • Ensure all responses are accurate, current, non-promotional, and aligned with applicable regulations and company policies.

  • Support global and regional medical information activities across therapeutic areas.

Medical Enquiry Management

  • Lead the development and maintenance of:

    • Standard Response Documents (SRDs)

    • Customized medical enquiry responses

    • Frequently Asked Questions (FAQs)

    • Off-label information responses

    • Complex scientific and medical communications

  • Ensure timely and accurate responses to unsolicited medical enquiries.

  • Address complex clinical and scientific questions using available evidence and medical literature.

Literature Review & Evidence Synthesis

  • Conduct comprehensive literature searches using scientific databases and medical journals.

  • Critically evaluate, analyze, and summarize scientific publications.

  • Synthesize clinical and scientific evidence to support medical communication materials.

  • Maintain awareness of emerging clinical data, treatment guidelines, and competitive intelligence.

Quality & Regulatory Compliance

  • Ensure all medical information materials comply with regulatory requirements, industry guidelines, and company standards.

  • Participate in medical, legal, and regulatory review processes.

  • Maintain documentation and version control for all medical information content.

  • Support audit and inspection readiness activities as required.

Cross-Functional Collaboration

  • Collaborate with Medical Affairs, Pharmacovigilance, Regulatory Affairs, Clinical Development, and Commercial teams.

  • Provide scientific support to internal stakeholders regarding products, therapeutic areas, and clinical data.

  • Participate in content review meetings and strategic medical communication initiatives.

  • Support knowledge-sharing and training activities within the organization.

Continuous Improvement

  • Contribute to process optimization and enhancement of medical information workflows.

  • Identify opportunities to improve response quality, efficiency, and scientific consistency.

  • Stay current with therapeutic area developments, scientific literature, and healthcare regulations.


Required Qualifications

Education

  • Bachelor's degree in Pharmacy, Life Sciences, Medicine, Nursing, Biotechnology, or a related healthcare discipline.

  • Advanced degree such as PharmD, M.Pharm, PhD, MD, or equivalent is preferred.

Experience

  • 4–8 years of experience in Medical Information, Medical Affairs, Scientific Writing, Medical Communications, or related life sciences functions.

  • Experience developing medical enquiry responses and scientific communication materials.

  • Experience working within pharmaceutical, biotechnology, CRO, or healthcare organizations.