Pharmacovigilance Specialist (MD/PharmD) | Argus/Veeva | WFH

Cognizant; Taguig; Remote; PHP 500,000 - 900,000; Full time

Job summary

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

Key responsibilities include reviewing and validating medical information, providing expert clinical judgment, and collaborating with cross-functional teams to support decision-making and maintain medical review integrity.

Qualifications

• Minimum 2 years of experience in medical review of ICSSRs in safety databases like Veeva Safety and Argus.
• Fluency in English.
• Graduate/Postgraduate/Doctorate degree in Medical sciences or equivalent/MD.

Responsibilities

• Ensure scientific, clinical, and regulatory accuracy of medical and safety-related content across pharmacovigilance and healthcare activities.
• Review, assess, and validate medical information for compliance with global regulatory requirements and internal standards.
• Provide expert clinical judgment in evaluating adverse events, safety data, and medical narratives.

Skills

Fluency in English

Attention to detail

Medical terminology familiarity

Education

Graduate/Postgraduate/Doctorate degree in Medical sciences or equivalent

Bachelor of Medicine/MD

Job description

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 ICSSRs 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.