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Md/Do - Assoc Medical Mgr Pss / Pv Remote

4+ years
$70,000–$90,000 USD annually
10 July 31, 2025
Job Description
Job Type: Full Time Education: MD or 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 (MD/DO) – Pharmacovigilance | Remote – US/Canada

Job Summary:
Fortrea, a leading global CRO, is hiring a skilled Associate Medical Manager (MD/DO) to join its Patient Safety Solutions (PSS) team. This remote-based pharmacovigilance role is ideal for healthcare professionals with experience in drug safety, post-marketing surveillance, and clinical research. You will engage in case review, quality control, and compliance-driven safety deliverables across therapeutic areas. If you're looking to make an impact in global drug safety from a remote setting, this is your chance.


Key Responsibilities:

  • Conduct medical review of adverse event cases including seriousness, causality, and narrative assessments

  • Provide expert safety analysis for sponsor drugs, devices, and combination products

  • Perform QC and QA reviews of case data to ensure quality and compliance

  • Offer guidance and training to case processing teams

  • Track deliverables and documentation using tools and trackers

  • Participate in ongoing improvement initiatives and cross-functional collaboration

  • Interpret clinical research protocols and contribute to medical training sessions

  • Support post-marketing safety and global PV regulations adherence


Required Skills & Qualifications:

  • MD or DO with at least 4 years of pharmacovigilance experience

  • Strong clinical trial and post-approval drug safety knowledge

  • Deep understanding of US healthcare system and regulatory landscape

  • Familiarity with ICH-GCP, case processing, and global PV requirements

  • Preferred: Accredited residency, board eligibility/certification

  • English proficiency in reading, writing, and speaking

  • 1–2 years of hands-on clinical practice is a plus


Perks & Benefits:

  • Salary:

    • US-based: $70,000–$90,000 USD annually

    • Canada-based: CAD 95,000–115,000 annually

  • Comprehensive benefits package (eligibility for employees working 20+ hours/week) including:

    • Medical, Dental, Vision, Life Insurance

    • Short & Long-Term Disability (STD/LTD)

    • 401(K), ESPP

    • Paid Time Off (PTO) or Flexible Time Off (FTO)

    • Performance-based company bonus (where applicable)


Company Overview:

Fortrea is a global contract research organization (CRO) offering advanced drug development and clinical solutions to pharmaceutical, biotech, and medical device companies across 100+ countries. Known for scientific excellence and innovation, Fortrea delivers transformative results across 20+ therapeutic areas with speed and compliance.


Work Mode: Remote (based in the United States or Canada)


Apply Now

Ready to drive global drug safety from anywhere in North America? Join Fortrea’s leading pharmacovigilance team. Apply today before the August 1, 2025 deadline to begin your next impactful chapter in the pharmaceutical industry.

Apply Now at ThePharmaDaily.com