About the role

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

Apply now and bring your medical expertise to a role where your clinical judgment helps shape safer healthcare outcomes worldwide.

Licensed Physician | Pharmacovigilance Specialist | Argus/Veeva