Cencora Hiring for Senior Specialist- Pharmacovigilance Role: PV Jobs 2026
Cencora, a global healthcare services and pharmaceutical solutions organization, is hiring for the role of Senior Specialist – Pharmacovigilance at its Noida location. This opportunity is suitable for candidates with a B.Pharm or M.Pharm degree and 2 years of hands‑on experience in pharmacovigilance and ICSR case processing.
The role focuses on end‑to‑end safety case management, regulatory compliance, and supporting global pharmacovigilance operations within a structured and regulated environment. Candidates will work closely with cross‑functional safety teams to ensure accurate, timely, and compliant handling of adverse event data.
🏢 About Cencora
Cencora is a global healthcare services organization supporting pharmaceutical and life sciences companies across regulatory, pharmacovigilance, and clinical operations. The organization works within strict global safety and compliance standards and partners with clients to ensure patient safety and regulatory adherence throughout the product lifecycle. Working at Cencora offers exposure to global PV operations and complex safety workflows.
📊 Position Details
- Position: Senior Specialist- Pharmacovigilance
- Department: PV
- Location: Noida, India
- Experience: 2+ Years
- Qualification: B.Pharm, M.pharm
- Job Type: Full-Time
- Last Date to apply: 12 May2026
📋 What You Will Do– Senior Specialist- Pharmacovigilance
- Literature Screening & Monitoring
- Screen scientific and biomedical literature using internal search systems and approved external tools or service providers.
- Track and manage the internal literature ordering process to ensure timely retrieval of required publications.
- Safety Literature Classification & Data Entry
- Classify safety‑relevant publications according to established pharmacovigilance criteria.
- Perform accurate data entry of literature cases into the pharmacovigilance safety database.
- ICSR Processing & Documentation
- Prepare standard regulatory reporting forms such as CIOMS I, MedWatch forms, and relevant XML files.
- Complete case processing activities including case completion, review, and documentation.
- EMA MLM & Duplicate Check Activities
- Download, review, and distribute client‑specific ICSRs from the EMA Medical Literature Monitoring (MLM) service.
- Perform duplicate searches for literature cases using updated information available in the EMA MLM system.
- Client & Project Coordination
- Act as the primary point of contact for clients and project management teams regarding safety literature and ICSR activities.
- Cross‑Service Support
- Support additional pharmacovigilance service lines and related tasks, as required, in alignment with skills, training, and qualifications
🎓Who Can Apply
- Candidates must meet the following requirements:
- Bachelor’s or University degree in:
- Life Sciences
- Pharmacy
- Or a related scientific discipline
- Minimum 2+ years of experience in Pharmacovigilance, specifically ICSR processing
- Experience working in regulated PV environments preferred
🧠 Key Skills
- Strong written and verbal communication skills with a good command of the English language.
- Organizational & Problem‑Solving Skills: Effective organizational, planning, and problem‑solving abilities to manage multiple study tasks.
- Time & Financial Management:Capable of managing time, priorities, and site‑level financial activities efficiently.
- Professional Relationships: Ability to establish and maintain effective working relationships with study sites, coworkers, managers, and clients.
⭐ Work Insight
The Senior Specialist – Pharmacovigilance role is critical in ensuring patient safety and regulatory compliance throughout the drug lifecycle. Professionals in this role take ownership of safety case workflows, support junior team members, and act as key contributors to quality and compliance outcomes. This position is ideal for PV professionals aiming to move into senior operational or leadership‑track roles in drug safety.
🎯 Suitable For
This opportunity is suitable for:
- Pharmacovigilance professionals with 2+ years ICSR experience
- PV Specialists seeking senior‑level responsibilities
- Candidates experienced in safety case processing and coordination
- Professionals looking to grow within global PV organizations
📈Career Path
With experience and performance, professionals can progress into roles such as:
- Lead Pharmacovigilance Specialist
- PV Team Lead
- Drug Safety Manager
- PV Quality or Compliance Lead
Cencora also supports professional development and long‑term career growth paths.
💰 Salary Range
- Expected Salary:600000 to 750000. As per company standards for senior PV roles
💡Application Tips
- Highlight leadership, organization, and problem‑solving experience
- Revise ICSR workflows and safety reporting regulations
- Strengthen communication and stakeholder management skills
- Be prepared to discuss handling of multiple safety cases
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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❓FAQ-Senior Specialist- Pharmacovigilance
1. Who can apply for the Senior Specialist – Pharmacovigilance role at Cencora?
Candidates with a B.Pharm or M.Pharm degree and at least 2 years of experience in pharmacovigilance and ICSR case processing are eligible to apply.
2. What type of pharmacovigilance activities will I handle in this role?
You will manage literature screening, ICSR processing, duplicate checks, safety data entry, regulatory reporting, and documentation aligned with global PV requirements.
3. Is this role focused on literature monitoring?
Yes. The role includes screening scientific literature, classifying safety‑relevant publications, and working with the EMA Medical Literature Monitoring (MLM) system.
4. What safety systems or tools will I work with?
You will work with pharmacovigilance safety databases, internal search systems, EMA MLM services, and tools used for CIOMS I, MedWatch, and XML reporting.
5. Will I be responsible for client interactions?
Yes. You will act as a primary point of contact for assigned clients and project management teams for literature and ICSR‑related activities.
