Cencora, a global healthcare services leader and parent organization of PharmaLex, is actively hiring experienced professionals across Pharmacovigilance, Drug Safety, Epidemiology, Risk Management, and Safety Database Operations. These full-time roles are based in Noida, India, and offer long-term career growth in a global regulatory environment.
If you are a Drug Safety Physician, Medical Reviewer, Pharmacovigilance Manager, or Safety Database Professional, this is a strong opportunity to work with global clients, regulatory authorities, and advanced PV systems.
Open Positions at Cencora (Noida)
- Manager, Drug Safety Physician – Pharmacovigilance, Epidemiology & Risk Management
- Manager, Drug Safety Physician – Pharmacovigilance
- Manager – Case Processing (Pharmacovigilance)
- Medical Reviewer – Case Processing
- Manager – Safety Database (PV Systems)
Key Responsibilities (Role-Dependent)
Pharmacovigilance & Medical Review Roles
- Medical review and assessment of Individual Case Safety Reports (ICSRs)
- Verification of adverse events, seriousness, causality, MedDRA coding, narratives, and lab data
- Preparation and review of PSURs, PBRERs, and Risk Management Plans (RMPs)
- Scientific literature screening and medical triage
- Signal detection collaboration with global PV teams
- Training and mentoring PV associates
- Participation in regulatory audits and inspections
- Compliance with ICH, EMA, FDA, GVP, and GCP guidelines
Safety Database & PV Technology Roles
- Configuration and administration of PV safety databases
- User access management and system maintenance
- Validation documentation (URS, FRS, IQ/OQ/PQ)
- GxP and 21 CFR Part 11 compliance
- Database migrations and system upgrades
- First-level technical support and audit readiness
- End-user training and documentation
Case Processing Management Roles
- End-to-end case processing and quality oversight
- Resource and workload management
- Staff recruitment, training compliance, and appraisals
- Client coordination and invoice management
- SOPs, WI, SDEAs drafting and review
- Regulatory submissions and compliance tracking
- Risk identification and workflow optimization
Qualifications & Experience
Education
- Medicine Degree (MBBS/MD) – Mandatory for Medical Reviewer & Drug Safety Physician roles
- Life Sciences / Pharmacy / Computer Science – For Safety Database and Case Processing roles
Experience Requirements
- 3–10+ years of experience in Pharmacovigilance & Drug Safety
- Strong hands-on experience with ICSR processing, medical review, or PV systems
- Prior exposure to CRO, Pharma, or Life Sciences corporate environments preferred
Skills
- Excellent written and spoken English
- Strong regulatory and compliance knowledge
- Leadership and mentoring capability
- High attention to detail and problem-solving mindset
- Ability to perform under regulatory timelines
Why Work at Cencora?
- Global exposure with regulated markets (EMA, FDA, MHRA)
- Stable full-time employment
- Hybrid and structured work environment
- Strong learning and leadership opportunities
- Equal Employment Opportunity employer
- Inclusive and compliance-driven workplace culture
How to Apply
Application Link For Manager, Drug Safety Physician – Pharmacovigilance
Application Link For Manager – Case Processing (Pharmacovigilance)
Application Link For Medical Reviewer – Case Processing
Application Link For Manager – Safety Database (PV Systems)
