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Medical Physician Specialist Ii – Mumbai

1-2 years
Not Disclosed
10 Nov. 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Medical Physician Specialist II – Mumbai

Full-Time | Job ID: 255708
Application Deadline: November 24, 2025

Job Overview

The Medical Physician Specialist II will provide advanced medical safety expertise in the post-marketing phase for pharmaceutical products, medical devices, and combination products. This role focuses on medical case evaluation, clinical safety decision-making, and ensuring regulatory-compliant pharmacovigilance practices.


Key Responsibilities

Medical Case Review

  • Conduct primary medical review of individual case safety reports, including seriousness assessment, labeling/listedness evaluation, causality assessment, adverse event coding, and narrative verification.

  • Complete daily documentation of case data and feedback using standardized trackers and workflow tools.

Quality, Compliance, and Delivery

  • Take full responsibility for all assigned safety deliverables in alignment with quality standards, regulatory compliance, productivity targets, and client SLAs/KPIs.

  • After one year of tenure, provide medical training and guidance to case processing teams.

Quality Control & Assurance

  • Perform secondary medical review (QC) and retrospective medical case evaluations (QA) after more than one year of service to identify error trends, training needs, and opportunities for process improvement.

Safety Surveillance

  • Support aggregate medical review processes and participate in signal detection and safety trend analysis as required.

Client Engagement & Process Improvement

  • Contribute to strengthening client relationships through consistent delivery and professional communication.

  • Promote a high-service culture and actively participate in internal process optimization initiatives.


Minimum Qualifications

  • Bachelor’s degree in Medical Science, or an MD/DO or equivalent medical qualification.

  • Relevant and equivalent experience may be considered in place of formal educational requirements.

  • Proficiency in English:

    • Speaking: ILR 3+

    • Reading/Writing: ILR 4+


Experience Required

  • Foundational understanding of medical sciences, diagnosis, therapeutics, and clinical procedures.

  • Knowledge of regulatory guidelines for clinical research and familiarity with ICH-GCP.

Preferred Experience

  • Up to 1 year of pharmaceutical industry experience, including pharmacovigilance (case processing or medical review) or clinical research.

  • 1 to 2 years of clinical practice experience.

  • Understanding of pharmacovigilance regulations and safety reporting requirements.


Work Environment

  • May be office-based or home-based depending on business needs and manager approval.