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Veeva Safety

Cognizant
Cognizant
3-10 years
preferred by company
10 Feb. 2, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Veeva Vault Safety Specialist – Pharmacovigilance Systems

Job ID: 00066982602
Location: Chennai, India
Work Model: Hybrid
Job Category: Technology & Engineering / Pharmacovigilance
Employment Type: Full-Time
Date Published: January 24, 2026
Company: Cognizant


About Cognizant

Cognizant is a global professional services leader helping organizations modernize technology, reimagine processes, and transform experiences for the digital era. With over 300,000 associates worldwide, Cognizant partners with leading life sciences and healthcare organizations to deliver innovative, compliant, and scalable solutions. Recognized among Forbes World’s Best Employers 2025, Cognizant fosters an inclusive, high-performance, and future-ready workplace.


Role Overview

Cognizant is seeking an experienced Veeva Vault Safety Specialist to manage and optimize pharmacovigilance systems supporting global drug safety operations. This role is responsible for the configuration, maintenance, and regulatory compliance of Veeva Vault Safety, ensuring accurate safety data processing and reporting in line with international regulations.

The position requires strong expertise in pharmacovigilance systems, safety reporting workflows, and cross-functional collaboration within clinical development environments.


Key Responsibilities

Veeva Vault Safety System Management

  • Oversee day-to-day operation, administration, and maintenance of the Veeva Vault Safety platform.

  • Configure and customize system workflows to meet organizational needs and global regulatory requirements.

  • Implement and manage workflows for adverse event reporting, risk management, and safety signal tracking.

  • Ensure ongoing compliance with global pharmacovigilance regulations including FDA, EMA, and ICH guidelines.

  • Monitor regulatory updates and implement system enhancements accordingly.

Safety Data Management & Reporting

  • Manage the collection, processing, and quality review of safety data across clinical and post-marketing programs.

  • Prepare, review, and submit periodic safety reports and regulatory deliverables within defined timelines.

  • Generate safety metrics, dashboards, and analytical reports for internal and external stakeholders.

  • Ensure data integrity, confidentiality, and audit readiness of safety databases.

Cross-Functional Collaboration

  • Work closely with Clinical Operations, Regulatory Affairs, IT, and Quality teams to optimize system usage.

  • Participate in cross-functional safety review meetings to evaluate trends, risks, and compliance issues.

  • Contribute to continuous improvement initiatives for pharmacovigilance processes and systems.


Education & Qualifications

  • Bachelor’s or Master’s degree in Pharmacy, Nursing, Life Sciences, or a related discipline.


Experience Required

  • 3 to 10 years of experience in pharmacovigilance, drug safety, or safety systems management.

  • Hands-on experience with Veeva Vault Safety or similar pharmacovigilance platforms is strongly preferred.

  • Demonstrated knowledge of global safety reporting regulations and submission requirements.


Key Skills & Competencies

  • Veeva Vault Safety configuration and administration

  • Global pharmacovigilance compliance (FDA, EMA, ICH)

  • Safety data management and regulatory reporting

  • Strong analytical and problem-solving abilities

  • Excellent communication and stakeholder management skills

  • Ability to work independently and within cross-functional teams


Why Join Cognizant

  • Work with a global leader in life sciences digital transformation.

  • Hybrid work model supporting flexibility and work-life balance.

  • Competitive compensation and benefits aligned with local market standards.

  • Inclusive, collaborative, and innovation-driven workplace culture.

  • Clear career growth pathways across pharmacovigilance, technology, and regulatory domains.


Equal Opportunity Statement

Cognizant is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, gender, disability, sexual orientation, or any other legally protected status. Reasonable accommodations are available throughout the hiring process.


Apply Now

If you are a pharmacovigilance professional with strong Veeva Vault Safety expertise and a passion for global drug safety compliance, apply today to advance your career with Cognizant.