Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Medical Physician Specialist I

Fortrea
Fortrea
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.