Licensed Physician | Pharmacovigilance Specialist | Argus/Veeva
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Medical Abstractor at SME level working from home. The role involves ensuring the scientific, clinical, and regulatory accuracy of medical and safety-related content across pharmacovigilance and healthcare activities.
Key Responsibilities
- Conduct medical review and validation of Individual Case Safety Reports (ICSRs) , adverse event reports, and safety data within Argus and Veeva Safety platforms.
- Provide clinical expertise and scientific assessment to support pharmacovigilance activities, safety evaluations, and risk management initiatives.
- Review medical narratives, interpret clinical data, and identify potential safety signals to ensure accurate and compliant safety reporting.
- Partner with global Pharmacovigilance, Regulatory Affairs, Clinical Operations, and Quality teams to maintain the highest standards of patient safety and regulatory compliance.
- Serve as a subject matter expert for complex cases and contribute to continuous process improvement and quality initiatives.
Qualifications
Doctor of Medicine (MD)
Minimum 2 years of experience in Pharmacovigilance Medical Review and ICSR evaluation
Hands-on experience with Argus Safety and/or Veeva Safety
Strong knowledge of drug safety, adverse event reporting, and global pharmacovigilance regulations
Excellent English communication and medical writing skills
Ability to thrive in a collaborative, fully remote work environment
Why Join Us?
- Permanent Work From Home Setup
- Collaborate with global healthcare and life sciences teams
- Opportunities for career growth and specialization in Drug Safety & Pharmacovigilance
- Play a critical role in protecting patient safety worldwide
- Work on complex and impactful medical review cases in a highly regulated environment
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