Senior Specialist Pharmacovigilance Job at Cencora in Noida. Apply for PV job with ICSR, literature review and safety database experience.
Introduction
Professionals with experience in pharmacovigilance and drug safety operations have a strong opportunity to advance their careers. Cencora is hiring for the role of Senior Specialist – Pharmacovigilance in Noida. This position is ideal for candidates with hands-on experience in literature screening, ICSR handling, and safety database management.
Company Overview
Cencora is a global healthcare services organization focused on improving patient outcomes and ensuring safe access to medicines. The company operates across pharmaceutical distribution, clinical services, and regulatory support. In India, its affiliated entity PharmaLex India Private Limited plays a key role in delivering pharmacovigilance and regulatory solutions.
Job Location & Employment Type
- Location: Noida, Uttar Pradesh, India
- Job Type: Full-Time
- Industry: Pharmacovigilance / Drug Safety
Job Overview (Job Details Table)
| Job Title | Senior Specialist – Pharmacovigilance |
|---|---|
| Company Name | Cencora (PharmaLex India Private Limited) |
| Qualification | Degree in Life Sciences |
| Experience | Minimum 2 Years |
| Job Location | Noida, Uttar Pradesh |
| Employment Type | Full-Time |
| Salary | As per company norms |
| Application Mode | Online Application |
| Department | Pharmacovigilance / Drug Safety |
Open Positions / Department Details
The position is part of the Pharmacovigilance and Drug Safety Department, where the selected candidate will work on literature monitoring, case processing, and regulatory reporting activities. The role involves collaboration with global teams and clients.
Key Roles & Responsibilities
As a Senior Specialist in Pharmacovigilance, your responsibilities will include:
- Screening scientific literature using internal systems and external databases
- Identifying and classifying safety-relevant publications
- Managing literature tracking and ordering processes
- Entering literature-based case data into safety databases
- Preparing regulatory reporting documents such as:
- CIOMS I forms
- MedWatch forms
- XML safety reports
- Performing case processing and ensuring proper documentation
- Downloading and reviewing ICSRs from EMA’s Medical Literature Monitoring (MLM) service
- Conducting duplicate checks for literature cases
- Acting as a primary contact point for client communication and project coordination
- Supporting additional pharmacovigilance activities as required
Eligibility Criteria
Educational Qualification
- Bachelor’s or Master’s degree in Life Sciences or related field
Experience Required
- Minimum 2 years of experience in Pharmacovigilance
- Hands-on experience in:
- Literature screening
- ICSR processing
- Safety database handling
Skills Required
- Good understanding of pharmacovigilance principles and workflows
- Knowledge of literature review and case processing
- Familiarity with global regulatory reporting formats (CIOMS, MedWatch)
- Strong communication skills (written and verbal)
- Good presentation and documentation abilities
- Attention to detail and analytical thinking
- Ability to work in a team and handle client interactions
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in a global pharmacovigilance environment
- Exposure to international regulatory processes and clients
- Career growth in drug safety and PV operations
- Professional and inclusive work culture
Selection Process
The recruitment process may include:
- Application Screening
- Technical Interview (Pharmacovigilance Focus)
- Client/Project Discussion Round
- HR Interview
- Final Selection
Candidates with strong PV experience and literature handling expertise will have an advantage.
How to Apply
Interested candidates should apply through the official online application portal of the company. Ensure your resume includes:
- Pharmacovigilance experience details
- Knowledge of ICSR processing and literature review
- Experience with safety databases
Important Dates
- Application Deadline: Not specified (apply as soon as possible)
Why Apply for This Pharma Job?
This role offers excellent exposure for professionals aiming to grow in pharmacovigilance:
- Work with a global healthcare services organization
- Gain experience in literature monitoring and ICSR management
- Enhance expertise in regulatory reporting and compliance
- Opportunity to interact with international clients and teams
- Build a strong career path in drug safety and pharmacovigilance
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any company or recruiter. Candidates are advised to verify all details independently before applying. We do not charge any fee for job applications.
Final Call-to-Action
If you have experience in pharmacovigilance and want to advance your career in drug safety operations, apply online at the earliest. This opportunity at Cencora can help you grow in a global and highly specialized domain.
