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Medical Reviewer

0-2 years
₹20–28 LPA
10 Aug. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Medical Reviewer – Patient Safety
Location: Gurgaon, Haryana, India
Estimated Salary: ₹20–28 LPA (based on industry standards for Medical Reviewer roles in India)

At Baxter, every role contributes to saving and sustaining lives. As a global leader in healthcare solutions, our products and therapies can be found in nearly every hospital, clinic, and home worldwide. For over 85 years, we have pioneered significant medical innovations that continue to transform patient care.

We are seeking a Medical Reviewer who will provide medical oversight on pharmacovigilance activities, ensuring safety, compliance, and regulatory excellence.

Key Responsibilities:

  • Provide medical review for individual case safety reports (ICSRs) including coding, seriousness, expectedness, and causality assessment.

  • Ensure consistency and sound medical interpretation in adverse event case assessments.

  • Contribute to periodic documents and product label reviews.

  • Support the Safety Operations team on medical questions such as event coding, case splitting, and coding conventions.

  • Maintain up-to-date knowledge of global regulatory guidelines (FDA, EMA, and others).

  • Provide medical/scientific expertise on pharmacovigilance matters for regulatory submissions.

  • Contribute to training, education, and leadership within the department.

  • May perform benefit–risk analyses, safety surveillance, risk management planning, and preparation of regulatory assessment reports and queries.

Qualifications & Skills:

  • Medical degree (or equivalent) with board certification/eligibility.

  • At least 2 years post-residency, with minimum 1 year in pharmaceutical/biotechnology industry.

  • Experience with adverse event processing, global regulations, and drug safety practices.

  • Familiarity with commercial safety databases and dictionaries (MedDRA, WHOART, COSTART, etc.).

  • Strong oral/written communication and presentation skills.

  • Ability to collaborate effectively across global, cross-functional teams.

  • Prior exposure to regulatory authority interactions (FDA, EMA, etc.) preferred.

What We Offer:

  • Future-focused and flexible workplace (minimum 3 days onsite per week).

  • Additional annual leave benefits.

  • Value-driven and collaborative culture where you can make a global impact.

Baxter is an equal opportunity employer committed to workplace inclusivity and reasonable accommodations for individuals with disabilities.