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Medical Physician Specialist I

1-2 years
Not Disclosed
10 June 11, 2025
Job Description
Job Type: Full Time Education: MBBS, MD, DO 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

 

Job Summary

Fortrea is seeking a Medical Physician Specialist I to deliver expert medical safety oversight in the post-marketing phase of drugs, devices, and combination products. The role involves in-depth medical case reviews, causality assessments, and signal analysis to ensure regulatory compliance and patient safety. This is an On-site or Remote opportunity offering involvement in global pharmacovigilance operations for pharmaceutical and medical device projects.


Key Responsibilities

  • Conduct comprehensive medical assessments of individual safety cases including seriousness, labeling/listedness, causality evaluation, AE coding, and narrative review.

  • Update and document daily case data and feedback using tracking tools for workflow management.

  • Take full accountability for the quality, compliance, and productivity of assigned deliverables as per SLAs and KPIs.

  • Provide training and guidance on medical aspects of case processing after completing one year in the role.

  • Support aggregate data and signal detection analysis when required.

  • Foster a strong culture of customer service and professional collaboration.


Required Skills & Qualifications

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

  • 1–2 years of clinical practice experience preferred.

  • Strong working knowledge of medical sciences, therapeutic areas, diagnosis, and pharmacotherapy.

  • Familiarity with global clinical research regulations, including ICH-GCP guidelines.

  • Proficient English communication skills (Speaking: ILR 3+; Reading/Writing: ILR 4+).

  • Ability to interpret complex clinical data and regulatory requirements effectively.

  • Willingness to work in an office or remote setting as per project needs.


Perks & Benefits

  • Opportunity to work with a leading global CRO.

  • Exposure to global pharmacovigilance and clinical safety standards.

  • Flexible work arrangement – On-site or Remote options.

  • Professional growth through continuous learning and global collaborations.

  • Be part of cutting-edge drug and device safety initiatives.


Company Description

Fortrea is a top-tier global Contract Research Organization (CRO) delivering clinical development, technology, and safety solutions across 20+ therapeutic areas. With operations in nearly 100 countries, Fortrea partners with pharmaceutical, biotechnology, and medical device companies to advance healthcare worldwide.


Work Mode

Remote or On-site (Multiple Locations)


Call-to-Action

Join Fortrea’s global safety science team to shape the future of drug and device safety. Apply now to contribute your medical expertise to life-changing healthcare innovations.