Cognizant has announced an opportunity for a Specialist (SPE) – Pharmacovigilance in Mumbai. The position is focused on pharmacovigilance data management, PV case processing, adverse event documentation, drug safety monitoring and regulatory compliance.
This Cognizant pharmacovigilance job is particularly relevant to professionals with hands-on experience in pharmacovigilance and a strong background in pharmaceutical research and development. Candidates are expected to understand drug safety processes, manage pharmacovigilance data accurately and collaborate with cross-functional and global teams.
The position follows a hybrid work model, operates during day shifts and does not require travel according to the job description.
Job Overview
| Particular | Details |
|---|---|
| Company | Cognizant |
| Position | SPE – Pharmacovigilance |
| Job ID | 00067689992 |
| Location | Mumbai, Maharashtra |
| Work Model | Hybrid |
| Shift | Day Shift |
| Category | Technology & Engineering |
| Key Skills | Pharmacovigilance, PV Data Management, Case Processing, Drug Safety |
| Experience | Hands-on pharmacovigilance experience required |
| Application | Online |
Key Responsibilities
Selected candidates for the Cognizant Pharmacovigilance Specialist job will be responsible for:
- Monitoring and evaluating drug safety data in accordance with regulatory standards and company procedures.
- Managing pharmacovigilance data and supporting accurate PV case processing.
- Reviewing and documenting adverse event reports and safety assessments accurately and on time.
- Collaborating with cross-functional teams to analyze and interpret pharmacovigilance data.
- Developing strategies to improve PV case processing and data-management efficiency.
- Providing data-driven recommendations to support pharmaceutical product safety and efficacy.
- Supporting the preparation of regulatory submissions and drug safety reports.
- Conducting audits of pharmacovigilance processes and identifying opportunities for quality improvement.
- Supporting training activities to strengthen team knowledge of pharmacovigilance practices.
- Using relevant PV tools and methodologies to improve safety-data collection and analysis.
- Coordinating with global teams to maintain consistency in pharmacovigilance operations.
- Supporting risk-management plans and safety-monitoring strategies.
- Staying current with evolving pharmacovigilance regulations and industry practices.
Qualifications & Eligibility
Cognizant’s posting does not specify a particular academic degree. Instead, it emphasizes relevant professional knowledge and hands-on pharmacovigilance experience.
Candidates should have:
- A strong background in Pharma Research & Development.
- Hands-on experience in pharmacovigilance.
- Expertise in PV data management and case processing.
- Strong understanding of drug safety and adverse event documentation.
- Ability to analyze complex pharmacovigilance data and generate actionable insights.
- Proficiency with relevant pharmacovigilance software and tools.
- Strong analytical and problem-solving capabilities.
- Effective written and verbal communication skills.
- Ability to collaborate with cross-functional and global teams.
- A proactive approach to identifying and resolving drug-safety issues.
Certifications Required
The job posting lists the following certifications:
- Certified Pharmacovigilance Professional (CPP)
- Advanced Pharmacovigilance Certification
Candidates should verify the exact certification requirement on the official application page before applying.
Who Should Apply?
This opportunity is best suited to experienced pharmacovigilance professionals, particularly candidates working in PV case processing, drug safety, safety data management or related pharmaceutical R&D functions.
The original job description requires hands-on pharmacovigilance experience; therefore, this position should not be presented as a fresher opening unless Cognizant separately confirms fresher eligibility.
Key Skills for Cognizant Pharmacovigilance Role
Important skills include:
Pharmacovigilance | Drug Safety | PV Case Processing | PV Data Management | Adverse Event Reporting | Safety Assessment | Regulatory Compliance | Risk Management | Safety Reporting | Pharmaceutical R&D | Data Analysis | Quality Control
Benefits of This Opportunity
Based on the information provided in the official job description, candidates can expect:
- Hybrid working arrangement.
- Day-shift work schedule.
- No travel requirement.
- Exposure to global pharmacovigilance operations.
- Cross-functional collaboration.
- Experience in PV data management and case processing.
- Opportunities to work on drug safety, regulatory reporting and risk-management activities.
- Professional exposure within a large global technology and services organization.
Specific compensation and employee benefits for this Mumbai vacancy were not stated in the supplied job description and should be confirmed directly with Cognizant.
How to Apply
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