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Medical Physician Specialist Ii

1-2 years
Not Disclosed
10 Dec. 12, 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

Medical Physician Specialist II – Clinical Safety

Locations: Multiple (Office or Remote Options)
Category: Clinical
Job ID: 255797
Experience Required: 1–2 years in clinical practice or pharmacovigilance


Job Overview

We are seeking a Medical Physician Specialist II to provide expert medical safety oversight for Sponsors of drugs, medical devices, and combination products in the post-marketing phase. This role requires applying clinical knowledge to evaluate adverse events, ensure compliance with regulatory standards, and support pharmacovigilance activities.


Key Responsibilities

  • Conduct primary medical review of cases, including assessment of seriousness, causality, adverse event coding, narrative review, and alignment with labeling/listedness.

  • Update and document daily case data and feedback in trackers or workflow management systems.

  • Take ownership of all assigned deliverables, ensuring adherence to quality, compliance, and productivity SLAs/KPIs.

  • Provide training and guidance to case processing teams on medical aspects of case management (post 1 year of tenure).

  • Perform secondary medical review (QC) and retrospective case analysis (QA) to measure deliverable quality, identify trends, and suggest process improvements (after 1 year of tenure).

  • Conduct aggregate medical review and signal detection, as required for safety analysis.

  • Support and enhance client relationships while maintaining a high standard of customer service.

  • Participate in process improvement initiatives across the organization.


Minimum Qualifications

  • Bachelor’s degree in Medical Science, MD, DO, or equivalent. Relevant experience may be considered in lieu of formal education.

  • Strong knowledge of medical sciences, diagnosis, therapeutics, drug treatments, and clinical procedures.

  • Understanding of regulatory requirements for clinical research and ICH-GCP guidelines.

  • Proficiency in English communication: Speaking (ILR 3+), Reading/Writing (ILR 4+).


Preferred Qualifications

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

  • 1–2 years of clinical practice experience.

  • Familiarity with regulatory requirements related to pharmacovigilance.


Work Environment

  • Office or home-based work environment as per line manager requirements.

  • Adherence to Equal Employment Opportunity (EEO) and reasonable accommodations policies.


Why Join Us

This role offers an opportunity to apply clinical expertise in a global pharmacovigilance setting, contribute to drug and device safety, and advance your career in a high-impact, regulated healthcare environment.