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Medical Physician Specialist Ii

1-2 years
Not Disclosed
10 Oct. 19, 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

📍 Available in 2 Locations
Category: Clinical
Job ID: 255339


Job Overview

The Medical Physician Specialist II provides medical safety expertise to sponsors of drugs, medical devices, and combination products during the post-marketing period.
The role involves case review, safety analysis, signal detection, and collaboration with cross-functional teams to ensure high-quality pharmacovigilance (PV) deliverables.


Key Responsibilities

Medical Review & Assessment

  • Conduct primary medical review of safety cases, including:

    • Assessment of seriousness, listedness/labeling, and causality

    • Adverse event coding and narrative review

  • Perform aggregate medical review and signal detection/analysis as required

Documentation & Quality Oversight

  • Update and maintain daily case data and feedback trackers/tools for workflow management

  • Ensure compliance, quality, and productivity in all deliverables per SLAs and KPIs

  • Conduct secondary (QC) and retrospective (QA) reviews after 1+ year tenure to monitor quality and identify training needs

Training & Guidance

  • After completing 1 year in the role, provide medical training and guidance to the case processing team

  • Participate in process improvement initiatives and support knowledge sharing across teams

Client Collaboration

  • Strengthen existing client relationships through proactive communication and service excellence

  • Contribute to a culture of high customer service and accountability


Qualifications

Education (Minimum Required)

  • Bachelor’s degree in Medical Science, or

  • MD / DO (Doctor of Medicine / Doctor of Osteopathy), or equivalent degree

  • Fortrea may consider relevant and equivalent experience in lieu of education requirements.

Language Proficiency

  • Speaking: English at ILR Level 3+ or higher

  • Reading/Writing: English at ILR Level 4+ or higher


Experience

Minimum Required

  • Strong working knowledge of medical sciences, diagnosis, and therapeutics, including drug treatments and procedures

  • Understanding of regulatory requirements for clinical research

  • Familiarity with ICH-GCP (Good Clinical Practice) guidelines

Preferred

  • Good understanding of pharmacovigilance regulatory requirements

  • Up to 1 year of experience in the pharmaceutical industry, including pharmacovigilance or clinical research

  • 1–2 years of clinical practice experience


Work Environment

  • Office-based or home-based, depending on line manager’s discretion

  • Expected to maintain professional standards of confidentiality and compliance


Additional Information

  • Learn more about EEO & Accommodation requests here (link placeholder)

  • Employer: Fortrea — committed to advancing healthcare through innovation, collaboration, and quality research