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Manager – Medical Reviewer

5 years
20-25 LPA
5 Dec. 2, 2025
Job Description
Job Type: Full Time Education: MBBS/MD Pharmacology 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

Lambda Therapeutic Research Ltd. | Ahmedabad, India

Req ID: 1395
Posted On: 28 November 2025
Experience Required: Minimum 5 years
Annual CTC: INR 20,00,000 – 25,00,000


About Lambda Therapeutic Research Ltd.

Lambda Therapeutic Research Ltd. is a leading global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operational facilities in Mehsana (India), Warsaw (Poland), London (UK), Pittsburgh (USA), Las Vegas (USA), and Fargo (USA). With a workforce of over 1,500 professionals worldwide and more than two decades of expertise, Lambda offers comprehensive clinical trial services to the biopharmaceutical and generic pharmaceutical sectors.

The organization delivers end-to-end clinical research solutions backed by advanced technologies, therapeutic excellence, and strong scientific leadership. Lambda’s commitment to quality, performance, and innovation has established its reputation as a trusted global partner for clinical development programs.

Lambda values talent, integrity, and commitment, and continuously seeks skilled professionals who are driven to contribute to high-quality clinical outcomes.


Position Overview

The Manager – Medical Reviewer will lead key pharmacovigilance and signal management activities to support the safety evaluation of client medicinal products. The role requires deep scientific expertise, regulatory understanding, and the ability to influence cross-functional teams.


Key Responsibilities

  • Conduct ongoing signal detection for assigned medicinal products and evaluate benefit–risk profiles.

  • Collaborate with cross-functional signal detection teams to address issues, optimize methodologies, and improve review efficiency.

  • Provide expert input in preparing responses to regulatory authority inquiries or healthcare professional queries related to product safety.

  • Contribute to team training activities and knowledge enhancement initiatives.

  • Perform literature screening and review to identify ICSRs and relevant articles for signal assessment.

  • Conduct label comparison between client product labels and reference/innovator labels; provide evidence-based recommendations for updates.

  • Escalate urgent safety concerns to the Line Manager and QPPV in a timely manner.

  • Draft Health Hazard Assessment (HHA) reports and support safety documentation deliverables.


Experience Requirements

  • Minimum 5 years of experience in Pharmacovigilance, focusing on signal detection, PSUR/Periodic Benefit–Risk Evaluation, or related drug safety activities.


Educational Qualification

  • MBBS or MD in Pharmacology is mandatory.