Corporate Pharmacovigilance Job at Cognizant
Looking for a Pharmacovigilance Job in a Leading Global Healthcare Company? If you have a background in life sciences, pharmacy, or medicine and are interested in drug safety, this opportunity at Cognizant could be the right fit for you. The Corporate Pharmacovigilance Job in Noida role offers exposure to pharmacovigilance, medical safety reviews, and clinical data evaluation in a global pharmaceutical environment. You’ll work with cross-functional teams to ensure patient safety and regulatory compliance. Read on to learn about the eligibility, responsibilities, required skills, and benefits of this exciting career opportunity.
About the Company:
Cognizant is a leading global technology and professional services company headquartered in the United States. The company provides digital transformation, AI-driven solutions, engineering, and consulting services across industries, including healthcare and life sciences. With a strong presence worldwide, Cognizant supports pharmaceutical and healthcare organizations through advanced technology, clinical research, pharmacovigilance, and regulatory solutions while helping improve patient outcomes.
Job Details:
| Company | Cognizant |
| Job Title | TL-Medical Safety |
| Department | Medical Safety / Pharmacovigilance |
| Location | Noida, India |
| Employment Type | Full-Time |
| Qualification | Life Sciences, Pharmacy, Medicine, or related discipline |
| Experience | Relevant experience or training in Pharmacovigilance and Medical Safety |
| Reference Number | Job ID: 00069665551 |
Job Description:
The TL-Medical Safety position focuses on medical review and evaluation of safety data within pharmacovigilance operations. The role involves reviewing Individual Case Safety Reports (ICSRs), assessing seriousness and causality, and evaluating clinical relevance. You will work with clinical trial data, product labeling, and risk-benefit information to ensure accurate safety assessments.
This Non-Clinical Job requires collaboration with pharmacovigilance and cross-functional safety teams to maintain regulatory compliance and patient safety standards. The position also includes using the safety database, refining medical narratives, verifying coding, and participating in signal detection activities aligned with global pharmacovigilance regulations and standard operating procedures.
Key Responsibilities:
- Perform medical safety reviews of Individual Case Safety Reports (ICSRs).
- Assess case seriousness, causality, and clinical relevance.
- Conduct end-to-end safety case processing and medical evaluation.
- Review clinical trial data, product labels, and risk-benefit information.
- Refine case narratives and verify medical coding accuracy.
- Support signal detection and identification of emerging safety trends.
- Ensure compliance with global pharmacovigilance regulations and SOPs.
- Maintain complete documentation for audit readiness and regulatory inspections.
Eligibility Criteria for the Corporate Pharmacovigilance Job:
- Bachelor’s or Master’s degree in Medicine, or a related healthcare discipline.
- Relevant experience or training in Pharmacovigilance and Medical Safety.
- Understanding of clinical concepts and therapeutic areas.
Preferred Certification:
- Good Pharmacovigilance Practices (GVP)
- Drug Safety or Pharmacovigilance Certification
- Equivalent industry-recognized certification
Required Skills:
- Medical Safety Review and Pharmacovigilance Operations
- ICSR Assessment and Adverse Event Evaluation
- Clinical Data Interpretation and Risk-Benefit Assessment
- Medical Narrative Writing and MedDRA Coding Verification
- Signal Detection and Safety Database Management
- Regulatory Compliance and Documentation Skills
- Strong Analytical Skills and Attention to Detail
- Excellent Written and Verbal English Communication
Benefits of the Corporate Pharmacovigilance Job:
- Opportunity to work with one of the world’s leading technology and healthcare service companies.
- Hands-on experience in global pharmacovigilance and medical safety operations.
- Hybrid work model offering flexibility and work-life balance.
- Exposure to international pharmaceutical projects and regulatory standards.
- Career growth in pharmacovigilance, drug safety, and medical review.
- Continuous learning and professional development opportunities.
- Collaborative work environment with experienced healthcare professionals.
- Opportunity to contribute directly to patient safety and regulatory compliance.
