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Assistant Manager - Medical Reviewer

2+ years
INR 18,00,000 – 22,50,000
10 Oct. 7, 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

Job Title: Assistant Manager – Medical Reviewer

Req ID: 1396
Date Posted: October 2, 2025
Location: Ahmedabad, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 18,00,000 – 22,50,000


Organizational Overview

Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with operations in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK), and Warsaw (Poland).

Key Highlights:

  • Offers end-to-end clinical research services to global innovator, biotech, and generic pharmaceutical companies

  • Focused on quality, compliance, and innovation across all clinical research activities


Job Overview

The Assistant Manager – Medical Reviewer will ensure all pharmacovigilance (PV) activities comply with SOPs, global regulations, and industry standards. This role provides medical and regulatory guidance, supports safety data assessment, and contributes to the continuous improvement of PV processes.


Key Responsibilities

  • Ensure all pharmacovigilance activities adhere to SOPs, regulations, and industry guidelines

  • Provide expert medical and regulatory guidance to clients and internal teams

  • Support assessment and oversight of safety data

  • Contribute to the development and revision of SOPs, templates, and training materials

  • Mentor junior staff and deliver training

  • Provide backup medical support as needed

  • Evaluate adverse events, perform causality assessments, and review narratives

  • Ensure timely and compliant ICSR submissions

  • Communicate effectively with leadership for issue escalation and regulatory responses


Required Experience

  • Minimum 2 years clinical experience or relevant pharmacovigilance experience


Educational Qualification

  • MBBS


Skills & Competencies

  • Strong understanding of pharmacovigilance regulations and guidelines

  • Proficiency in adverse event assessment and ICSR reporting

  • Ability to mentor and train junior staff

  • Effective communication and regulatory intelligence skills

  • Collaborative approach with leadership and cross-functional teams