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
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