Medical Reviewer | Pharmacovigilance Specialist | Argus/Veeva | WFH
Company: Cognizant
- Location: Taguig, Philippines
- Seniority: Mid level
- Employment type: Full-time
- Posted: 5 days ago
- Offer language: English
Job description
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
- Ensure the scientific, clinical, and regulatory accuracy of medical and safety-related content across pharmacovigilance and healthcare activities.
- Conduct comprehensive review, assessment, and validation of medical information to ensure compliance with global regulatory requirements, internal quality standards, and industry best practices.
- Serve as a key medical authority by providing expert clinical judgment and guidance in the evaluation of adverse events, safety data, medical narratives, and other medically relevant documentation.
- Collaborate with cross-functional teams, including pharmacovigilance, clinical operations, regulatory affairs, quality assurance, and client stakeholders, to support decision-making and maintain the integrity of medical review processes.
- Interpret complex clinical data, identify potential safety concerns, ensure consistency in medical assessments, and provide evidence-based recommendations.
- Contribute to process improvement initiatives to enhance quality, efficiency, and compliance within medical review operations.
- Support training, mentoring, and knowledge-sharing activities for team members and stakeholders.
- Assist in resolving complex medical queries and provide subject matter expertise for challenging cases.
- Participate in audits, inspections, and quality reviews by offering medical and regulatory guidance.
- Bridge clinical expertise with operational execution to safeguard patient safety, maintain regulatory compliance, and ensure the delivery of high-quality medical review services.
Qualifications:
- Minimum 2 years of experience in medical review of ICSRs in safety databases like Veeva Safety and Argus.
- Fluency in English
- Graduate/Postgraduate/Doctorate degree in Medical sciences or equivalent degree
- Bachelor of Medicine/MD
Your future starts here—grow, thrive, and make an impact with Cognizant.
