PHARMAFull-time
SPE – Pharmacovigilance
MUMBAI (IN)HYBRIDPOSTED: 7/11/2026
PHARMAFull-time
HIRING ORGANIZATIONCOGNIZANTInformation Technology Services & Consulting
ROLE DEFINITION & RESPONSIBILITIES
Key Responsibilities
Perform end-to-end pharmacovigilance case processing.
Review clinical and post-marketing safety data.
Support signal detection and risk assessment.
Prepare accurate case narratives.
Assist regulatory reporting activities.
Maintain compliance with global PV regulations.
Participate in audits and quality initiatives.
Collaborate with cross-functional safety teams.
Preferred Qualifications
Degree in Pharmacy, Life Sciences, Medicine or related discipline.
2–4 years of Pharmacovigilance experience.
Experience in safety databases and PV workflows.
Knowledge of regulatory reporting.
Strong analytical and communication skills.
REQUIRED VERIFIED SKILLS
Pharmacovigilance
Case Processing
Safety Databases
PV Workflows
Regulatory Reporting
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Competitive compensation aligned with industry benchmarks for experienced drug safety professionals in India.
ORGANIZATION CONTEXT & CULTURE
Cognizant is a global professional services company that transforms clients' business, operating, and technology models for the digital era. They provide consulting, IT, and business process outsourcing services, focusing on helping clients adapt to rapid market changes and achieve digital transformation. Their offerings span across various industries, leveraging advanced technologies to deliver innovative solutions.
TEAM SIZE: 400,000+ employees
INDUSTRY: Information Technology Services & Consulting
EXPECTED CAREER ROADMAP
This role offers strong career progression within global healthcare projects, providing exposure to AI-driven healthcare technologies and pathways into senior subject matter expertise.
APPLICATION ADVISORY
Highlight your hands-on experience with end-to-end case processing and safety workflows. Focus on your familiarity with global PV regulations during the interview.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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