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Associate Medical Manager

1-2 years
Not Disclosed
10 July 31, 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

 

Associate Medical Manager – Clinical Safety (Pharmacovigilance)

Location: India (2 locations available)
Category: Clinical
Work Mode: Hybrid / On-site (based on line manager's request)


Job Summary

Fortrea is looking for an Associate Medical Manager with a strong background in medical science and pharmacovigilance. This role involves medical review of adverse events, signal detection, and providing key safety support in post-marketing drug and device environments. If you have expertise in ICH-GCP, clinical research, and a passion for patient safety, this is an excellent opportunity to contribute to global drug development with a top-tier CRO.


Key Responsibilities

  • Perform primary medical review of safety cases (seriousness, causality, coding, narratives)

  • Conduct secondary (QC) and retrospective (QA) medical review of processed cases

  • Guide and train case processors on medical aspects of pharmacovigilance

  • Document and update case details, feedback, and metrics in internal systems

  • Support signal detection and aggregate data reviews

  • Foster high-quality client interactions and enhance customer service culture

  • Participate in process improvement initiatives


Required Skills & Qualifications

  • Bachelor's degree in medical science, MD, DO, or equivalent

  • Fluent in English (spoken: ILR 3+; written: ILR 4+)

  • Strong knowledge of medical sciences, diagnosis, therapeutics, and procedures

  • Understanding of pharmacovigilance regulations and ICH-GCP guidelines


Preferred Qualifications

  • 1–2 years of pharmaceutical or clinical research industry experience

  • Up to 2 years of clinical practice experience

  • Knowledge of global PV regulatory requirements and safety reporting standards


Perks & Benefits

  • Opportunity to work in a globally recognized CRO with operations in 100+ countries

  • Exposure to post-marketing pharmacovigilance and regulatory compliance

  • Professional growth through leadership in safety case review and analysis

  • Collaborative, innovation-focused environment

  • Hybrid or on-site flexibility, depending on team needs


About Fortrea

Fortrea is a global contract research organization (CRO) that delivers top-tier clinical development and data-driven technology solutions to pharmaceutical, biotech, and medical device companies. With services spanning 20+ therapeutic areas and operations across nearly 100 countries, Fortrea is at the forefront of advancing patient care through science and innovation.


Call-to-Action

Ready to apply your medical expertise to global clinical safety? Join Fortrea today and take the next step in your career as an Associate Medical Manager. Submit your application now to contribute to impactful drug development and patient safety initiatives.