Instagram
youtube
Facebook

Medical Physician Specialist Ii – Mumbai & Pune

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 & Pune

Full-Time | Job ID: 255797
Application Deadline: November 24, 2025

Job Overview

This role provides specialized medical safety expertise for pharmaceutical and medical device Sponsors during the post-marketing phase. The Medical Physician Specialist II will contribute to medical case review, safety assessment, and regulatory-aligned pharmacovigilance activities, ensuring high-quality clinical safety outputs.

Key Responsibilities

Primary Medical Review

  • Conduct medical review of safety cases, including seriousness assessment, labeling/listedness evaluation, causality assessment, and narrative quality check.

  • Ensure accurate medical coding of adverse events and maintain documentation in designated safety systems and trackers.

Operational Excellence

  • Update daily case data and feedback in workflow and tracking tools for efficient case management.

  • Own all assigned deliverables, ensuring adherence to quality standards, compliance expectations, productivity metrics, SLAs, and KPIs.

Training & Quality Oversight

  • Provide medical guidance and training to case processing teams after completing one year of tenure.

  • Perform secondary medical review (QC) and retrospective case evaluation (QA), identifying quality issues, recurring trends, and training needs after exceeding one year of tenure.

Safety & Signal Activities

  • Support aggregate medical review, signal detection, and safety analysis activities as required.

  • Contribute to continuous improvement initiatives to elevate operational quality and client satisfaction.

Client Collaboration

  • Strengthen client relationships through effective communication and commitment to service excellence.

  • Promote a culture of accountability, customer service, and continuous improvement across the organization.


Minimum Qualifications

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

  • Candidates with relevant professional experience may be considered in lieu of educational criteria.

  • Strong proficiency in English (Speaking: ILR 3+ | Reading/Writing: ILR 4+).

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

  • Knowledge of regulatory requirements in Clinical Research and familiarity with ICH-GCP guidelines.


Experience Required

  • Minimum:

    • Working knowledge of medical sciences and regulatory expectations in clinical research.

  • Preferred:

    • Up to 1 year of experience in the pharmaceutical industry, 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

  • Position may be office-based or home-based based on business requirements and managerial guidance.