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Manager - Medical Reviewer

Lambda Therapeutic Research
Lambda Therapeutic Research
0-2 years
₹20,00,000 – ₹25,00,000 per annum
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Manager – Medical Reviewer

Company: Lambda Therapeutic Research Ltd.
Req ID: 1395
Location: Ahmedabad, India
Date Posted: 30 Oct 2025
CTC Range: ₹20,00,000 – ₹25,00,000 per annum


Company Overview

Lambda Therapeutic Research is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations in:

  • Mehsana (India)

  • Warsaw (Poland)

  • London (UK)

  • Pittsburgh (USA)

  • Las Vegas (USA)

  • Fargo (USA)

With over 1,500 employees globally, Lambda delivers full-spectrum clinical trial solutions with more than 20 years of experience in the biopharmaceutical and generic pharmaceutical industries. The organization leverages innovative technologies, therapeutic expertise, and a strong quality focus to help clients develop products safely, effectively, and efficiently.


Job Summary

The Manager – Medical Reviewer is responsible for performing signal detection and safety evaluation for client medicinal products, supporting regulatory interactions, and providing guidance on benefit-risk assessments and labeling. This role involves collaborating across functions to ensure timely and accurate pharmacovigilance deliverables.


Key Responsibilities

1. Signal Detection & Safety Assessment

  • Perform signal detection for client medicinal products to evaluate benefit-risk balance.

  • Conduct literature reviews to select relevant ICSRs and scientific articles.

  • Draft Health Hazard Assessment reports.


2. Collaboration & Communication

  • Interact with signal detection teams across multiple functional areas to resolve issues.

  • Provide input for responses to regulatory authorities or healthcare professionals on safety concerns.

  • Communicate urgent safety issues promptly to Line Manager and QPPV.


3. Labeling & Regulatory Support

  • Compare client product labels with reference/innovator labels and recommend labeling changes.

  • Assist in training team members on signal detection and pharmacovigilance processes.


Experience Required

  • Minimum 5 years in Pharmacovigilance or relevant signal detection/PSUR experience.


Educational Qualification

  • MBBS or MD in Pharmacology