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Medical Advisor – Internal Medicine

Pfizer
2+ years
INR 18 LPA – 30 LPA
Mumbai, India
1 July 2, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Basic Statistics Interpretation, Clinical Research Knowledge, Evidence Synthesis, Literature Review, Medical Writing, MS Word, Narrative Writing, Scientific Writing

Medical Advisor – Internal Medicine

Company: Pfizer
Location: Mumbai, India (Hybrid)
Department: Medical Affairs
Job Type: Full-Time


JOB OVERVIEW

The Medical Advisor – Internal Medicine is responsible for developing and executing medical strategies for assigned therapeutic products, providing scientific leadership, supporting regulatory and clinical initiatives, engaging with Key Opinion Leaders (KOLs), and collaborating with cross-functional teams to ensure compliant medical communications and evidence generation. The role serves as the medical expert for internal medicine products while supporting product lifecycle management, research, regulatory activities, and medical education.


KEY RESPONSIBILITIES

Medical Strategy

  • Develop and implement medical strategies for assigned products.

  • Align medical plans with business and therapeutic objectives.

  • Drive scientific initiatives across the product lifecycle.

  • Translate medical insights into actionable strategies.

Key Opinion Leader (KOL) Engagement

  • Build and maintain relationships with Key Opinion Leaders (KOLs).

  • Engage with healthcare professionals and medical societies.

  • Collaborate with academic institutions and government stakeholders.

  • Support advocacy initiatives in compliance with company policies.

Medical Affairs

  • Provide scientific and medical expertise for internal medicine products.

  • Review and approve scientific communication materials.

  • Deliver medical support for product lifecycle activities.

  • Respond to complex medical and scientific queries.

  • Ensure scientific accuracy of promotional and non-promotional materials.

Clinical Research & Evidence Generation

  • Lead local clinical research initiatives.

  • Support Real-World Evidence (RWE) studies.

  • Manage outcomes research projects.

  • Support Non-Interventional Studies (NIS).

  • Oversee Post-Marketing Surveillance (PMS) studies.

  • Contribute to investigator-initiated research.

Regulatory Affairs

  • Support product registrations and new indications.

  • Provide medical input for regulatory submissions.

  • Review product labeling documents.

  • Collaborate with regulatory affairs teams.

  • Support clinical data generation for regulatory requirements.

Scientific Communication

  • Review scientific publications and promotional materials.

  • Develop medical education content.

  • Ensure compliance with medical communication standards.

  • Support scientific presentations and educational initiatives.

Cross-Functional Collaboration

  • Partner with Commercial teams.

  • Collaborate with Regulatory Affairs.

  • Work closely with Clinical Development teams.

  • Support Marketing initiatives with scientific expertise.

  • Coordinate with Pharmacovigilance teams.

  • Collaborate with Market Access teams.

Medical Education & Training

  • Conduct scientific training for sales teams.

  • Provide therapeutic area education.

  • Develop internal medical training programs.

  • Support continuing medical education initiatives.

Compliance & Quality

  • Ensure compliance with company policies and SOPs.

  • Follow MAPP requirements.

  • Maintain regulatory compliance.

  • Support audit readiness.

  • Complete mandatory training requirements.


EDUCATIONAL QUALIFICATIONS

Required

  • Medical Degree (MBBS or equivalent).

Preferred

  • MD (Internal Medicine or related specialty).

  • Degree in Medical Sciences.

  • Postgraduate qualification in Medical Management.

  • Advanced Scientific Degree.


EXPERIENCE REQUIREMENTS

Required

  • Experience in Medical Affairs.

  • Pharmaceutical industry experience.

  • Experience supporting medical strategies.

  • Experience working with cross-functional teams.

Preferred

  • Internal Medicine therapeutic area experience.

  • Experience in clinical research.

  • Experience with regulatory submissions.

  • Experience in real-world evidence generation.

  • Experience engaging with KOLs.