Licensed Physician | Pharmacovigilance Specialist | Argus/Veeva

Cognizant; Taguig; A distancia; PHP 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

Cognizant is seeking a Medical Abstractor at the SME level to work from home in the Philippines. The role focuses on ensuring scientific, clinical, and regulatory accuracy of medical and safety content across pharmacovigilance activities.

The candidate will review ICSRs, adverse events, and safety data using Argus Safety or Veeva Safety, provide clinical assessments, and support risk management initiatives. Strong English writing skills are required.

Formación

• MD degree required.
• 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.

Responsabilidades

• Conduct medical review and validation of ICSRs and safety data.
• Provide clinical expertise to support pharmacovigilance activities and risk management.
• Review medical narratives, interpret clinical data, and identify potential safety signals.
• Collaborate with global teams to maintain patient safety and regulatory compliance.
• Serve as SME for complex cases and contribute to quality initiatives.

Conocimientos

Medical review

Pharmacovigilance

Scientific writing

Regulatory compliance

Educación

MD

Herramientas

Argus Safety

Veeva Safety

Descripción del empleo

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