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Medical Reviewer

TCS
3-10 years
INR 18 LPA – 45 LPA
Bangalore, Hyderabad, Mumbai, India
2 June 15, 2026
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill

Medical Reviewer

Location: Mumbai, Pune, Bengaluru, Hyderabad, India
Employment Type: Full-Time

Job Summary

The Medical Reviewer is responsible for the medical evaluation, assessment, and review of adverse event cases, clinical trial safety reports, spontaneous reports, and literature cases within the pharmacovigilance framework. The role involves performing comprehensive medical assessments, evaluating causality and seriousness, ensuring regulatory compliance, and contributing to patient safety throughout the product lifecycle.


Key Responsibilities

Medical Case Review & Assessment

  • Perform medical review of clinical trial, spontaneous, solicited, and literature adverse event cases.

  • Evaluate the medical accuracy, completeness, and consistency of safety cases.

  • Review and validate case narratives, medical histories, laboratory results, and clinical information.

  • Ensure accurate documentation of safety assessments and medical conclusions.

Safety Evaluation & Causality Assessment

  • Conduct medical assessments including:

    • Seriousness determination

    • Expectedness assessment

    • Causality assessment

    • Benefit-risk evaluation

  • Provide company causality statements in accordance with internal and regulatory requirements.

  • Assess adverse events and serious adverse events (AE/SAE) in the context of product safety profiles.

Medical Coding & Data Review

  • Review medical coding accuracy for adverse events, indications, medical history, and concomitant medications.

  • Ensure consistency between source documentation and safety database records.

  • Evaluate suspect products, concomitant therapies, laboratory findings, and patient outcomes.

  • Support quality review of pharmacovigilance case processing activities.

Pharmacovigilance & Regulatory Compliance

  • Ensure compliance with global pharmacovigilance regulations, company SOPs, and industry standards.

  • Support regulatory reporting and safety surveillance activities.

  • Participate in audits, inspections, and quality assurance initiatives.

  • Maintain accurate and audit-ready documentation.

Therapeutic Area Expertise

  • Develop and maintain expertise in assigned therapeutic areas and disease biology.

  • Monitor emerging safety information and scientific literature related to marketed and investigational products.

  • Provide medical insights on important safety concerns and risk management strategies.

  • Contribute to signal detection, safety evaluations, and benefit-risk assessments when required.

Cross-Functional Collaboration

  • Collaborate with Pharmacovigilance, Drug Safety, Medical Affairs, Clinical Development, Regulatory Affairs, and Quality teams.

  • Provide medical expertise to support safety case processing and regulatory submissions.

  • Participate in safety review meetings and cross-functional discussions.

  • Support training and mentoring of pharmacovigilance team members when required.

Quality & Continuous Improvement

  • Ensure high-quality medical review activities within established timelines.

  • Identify opportunities for process improvements and operational efficiencies.

  • Stay current with evolving pharmacovigilance regulations, medical practices, and industry trends.

  • Support implementation of best practices in medical review and drug safety operations.


Required Qualifications

Education

  • MBBS (Bachelor of Medicine and Bachelor of Surgery) – Mandatory.

  • MD (Doctor of Medicine) – Preferred.

Experience

  • 5–20 years of experience in Pharmacovigilance, Drug Safety, Medical Review, Clinical Research, or Medical Affairs.

  • Experience reviewing adverse event cases and performing medical safety assessments.

  • Experience working within pharmaceutical, biotechnology, CRO, or healthcare organizations.