Sr. Specialist Pharmacovigilance – Cencora Noida
Apply for Senior Specialist Pharmacovigilance at Cencora, Noida. PharmaLex India Pvt Ltd | Full-time | 2+ years experience | August 2025 openings.
At Cencora, we are driven by the mission to create healthier futures by improving healthcare delivery worldwide. We are currently seeking a Senior Specialist – Pharmacovigilance to join our team in Noida, India. This role offers an opportunity to work at the center of health innovation and contribute to global drug safety.
Company Overview
Cencora, together with PharmaLex India Private Limited, is a global leader in consulting, regulatory affairs, and pharmacovigilance services. Our team members play a critical role in supporting pharmaceutical and biotechnology organizations with safety monitoring, regulatory compliance, and advancing patient well-being. We foster a culture of inclusivity, collaboration, and continuous growth.
Job Role & Responsibilities
As a Senior Specialist in Pharmacovigilance, you will:
- Screen scientific literature using internal and external databases for safety-relevant publications.
- Classify and document references for pharmacovigilance activities.
- Manage the internal literature ordering process and ensure timely data entry into the safety database.
- Prepare reporting forms such as CIOMS I, MedWatch, and XML files.
- Perform case documentation and completion for accurate regulatory submission.
- Download, review, and share Individual Case Safety Reports (ICSRs) from EMA’s Medical Literature Monitoring (MLM) services.
- Conduct duplicate searches and maintain updated case records.
- Act as the primary contact for client communication and project management.
- Support additional tasks and cross-functional responsibilities within regulatory service lines when required.
Eligibility / Qualifications
- Education: Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related field.
- Experience: 1–3 years in pharmacovigilance, clinical safety, or regulatory publishing.
- Key Skills:
- Strong knowledge of regulatory guidelines (EMA/FDA).
- Proficiency in safety database entry and literature review.
- Familiarity with pharmacovigilance reporting standards.
- Excellent organizational, communication, and documentation skills.
- Experience with ISI Toolbox or other publishing tools preferred.
Location & Salary
- Location: Noida, Uttar Pradesh, India.
- Job Type: Full-time, Consulting (PharmaLex India Pvt Ltd).
- Salary & Benefits: Competitive package with health insurance, retirement plans, global employee assistance program, and flexible benefit options aligned with local market practices.
Application Process
Interested candidates can apply directly through the official link:
👉 Apply Here
Why Join Cencora?
- Be part of a global leader in healthcare consulting and pharmacovigilance.
- Work on international safety monitoring projects.
- Collaborative culture with growth-focused learning opportunities.
- Inclusive workplace offering equal employment opportunities for all.
FAQs
Q1: Who can apply for this role?
Candidates with a degree in Life Sciences, Pharmacy, Biotechnology, or related fields and 1–3 years of pharmacovigilance experience.
Q2: Is prior experience in pharmacovigilance mandatory?
Yes, candidates with prior PV or clinical safety experience are preferred.
Q3: What are the working hours and job type?
This is a full-time, office-based consulting role in Noida.
Q4: Does Cencora provide equal opportunities?
Yes, Cencora ensures a workplace free of discrimination and provides accommodations for individuals with disabilities.
Summary Table
| Company | Cencora (PharmaLex India Pvt Ltd) |
|---|---|
| Vacancies | Senior Specialist – Pharmacovigilance |
| Required Education | B.Pharm, M.Pharm, Life Sciences, Biotechnology |
| Experience | 1–3 years in Pharmacovigilance |
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