Cognizant Hiring for SPE – Pharmacovigilance | Mumbai, Bangalore & Hyderabad

Company: Cognizant
Job Title: SPE – Pharmacovigilance
Job ID: 00069891251
Job Locations: Mumbai, Maharashtra | Bangalore, Karnataka | Hyderabad, Telangana
Department: Pharmacovigilance / Drug Safety
Industry: Pharmaceutical / Clinical Research / IT Services
Job Type: As per official job posting
Experience: At least 1 year of relevant exposure to clinical or safety-related documentation
Qualification: Relevant educational background in pharmaceutical, life sciences, clinical research, or a related field, as specified by the employer
Work Model: Hybrid
Shift: Day shift

Job Description

Cognizant is hiring professionals for the position of SPE – Pharmacovigilance across Mumbai, Bangalore, and Hyderabad. This opportunity is suited to candidates with experience in pharmacovigilance, drug safety, clinical documentation, and adverse event case processing who are interested in contributing to global patient safety initiatives.

Selected candidates will support pharmacovigilance operations, ensure accurate safety data documentation, and help maintain compliance with applicable global regulatory requirements.

Key Responsibilities

• Perform end-to-end pharmacovigilance case processing and adverse event data entry.
• Review source documents and clinical data to ensure accuracy and completeness.
• Process spontaneous and solicited adverse event reports according to established procedures.
• Support Individual Case Safety Report (ICSR) assessment, narrative preparation, and regulatory reporting.
• Review case seriousness and expectedness within the scope of assigned responsibilities.
• Identify missing information, resolve data discrepancies, and coordinate with cross-functional teams.
• Monitor case-processing timelines, workload queues, and service-level requirements.
• Maintain compliance with standard operating procedures and global pharmacovigilance guidelines.
• Protect confidential patient information and maintain audit-ready documentation.
• Participate in training activities and contribute to continuous process improvement.

Eligibility Criteria

• At least one year of exposure to clinical or safety-related documentation.
• Basic understanding of pharmacovigilance and drug safety case-processing concepts.
• Familiarity with adverse event reporting, ICSR documentation, and medical narrative preparation.
• Strong attention to detail and documentation skills.
• Good written and verbal communication skills.
• Ability to work collaboratively in a regulated, hybrid work environment.
• Willingness to learn and develop expertise in pharmacovigilance operations.

Preferred Certification

Pharmacovigilance or drug safety training from recognized professional organizations, such as DIA or similar industry bodies, is preferred.

Job Locations

• Mumbai, Maharashtra
• Bangalore, Karnataka
• Hyderabad, Telangana

How to Apply

Interested and eligible candidates can review the complete job description and submit their applications through the official Cognizant careers portal.

Official Application Portal: https://careers.cognizant.com/global-en/jobs/

Job ID: 00069891251

Candidates should search for the job ID on the official careers website to locate the specific vacancy and verify its current application status.