Medical Reviewer Case Processing Job at Cencora. MBBS candidates with pharmacovigilance experience can work on ICSR review and drug safety.
Are you an experienced medical professional in pharmacovigilance looking for a senior-level role in drug safety? Cencora is hiring for the position of Medical Reviewer – Case Processing in Noida. This role is ideal for doctors with strong expertise in ICSR review, safety data evaluation, and regulatory compliance who want to work on global pharmacovigilance projects.
Company Overview
Cencora is a leading global healthcare services organization focused on improving patient outcomes through innovative pharmaceutical solutions. Through its affiliate PharmaLex India Private Limited, the company delivers specialized services in pharmacovigilance, regulatory affairs, and compliance. With a strong international presence, Cencora supports life sciences companies in ensuring drug safety and regulatory adherence.
Job Overview
| Job Title | Medical Reviewer – Case Processing |
|---|---|
| Company | Cencora (PharmaLex India Pvt. Ltd.) |
| Location | Noida, Uttar Pradesh, India |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Drug Safety |
| Experience | Minimum 8 Years |
| Qualification | MBBS (PG Preferred) |
| Application Deadline | July 30, 2026 |
| Job Requisition ID | R2522052 |
Job Location & Employment Type
- Work Location: Noida, Uttar Pradesh
- Job Type: Full-time
- Work Mode: Office-based / hybrid (as per company policy)
Open Positions / Department Details
This role is part of the Pharmacovigilance Case Processing and Medical Review team, focusing on safety case evaluation, ICSR review, and regulatory compliance.
Key Roles & Responsibilities
As a Medical Reviewer – Case Processing, you will be responsible for reviewing and validating drug safety cases with clinical accuracy.
Medical Review & Case Evaluation
- Performing medical review of Individual Case Safety Reports (ICSRs)
- Assessing adverse events for:
- Seriousness
- Expectedness
- Causality
- Verifying correct selection of:
- MedDRA coding
- Suspect drugs and concomitant medications
- Laboratory data and medical history
Safety Data Validation & Documentation
- Reviewing and refining case narratives
- Providing company causality comments
- Documenting review findings in safety databases
- Ensuring completeness and accuracy of safety data
Query Management & Case Follow-Up
- Responding to queries from case processors
- Identifying missing or incomplete information
- Recommending follow-up actions for additional data collection
Regulatory Compliance & Standards
- Ensuring compliance with:
- ICH guidelines
- EMA regulations
- FDA requirements
- Maintaining strong knowledge of GVP and GCP standards
- Supporting audit and inspection readiness
Training & Team Support
- Training and mentoring pharmacovigilance associates
- Sharing best practices for event capturing and case processing
- Supporting team development and knowledge enhancement
Communication & Collaboration
- Participating in internal project meetings
- Escalating complex safety issues to leadership
- Collaborating with cross-functional teams
Eligibility Criteria
Educational Qualification
Candidates must have:
- MBBS (Bachelor of Medicine, Bachelor of Surgery)
- Postgraduate degree (MD or equivalent) is preferred but not mandatory
Experience Required
- Minimum 8 years of experience in:
- Pharmacovigilance
- Drug safety
- Medical review of ICSRs
Skills Required
- Strong clinical knowledge and judgment
- Expertise in ICSR processing and medical review
- Knowledge of:
- MedDRA coding
- Safety databases
- Global regulatory guidelines
- Excellent communication and documentation skills
- Strong attention to detail and analytical skills
- Ability to work under pressure and meet deadlines
- Team collaboration and mentoring skills
Salary & Benefits
- Salary will be as per company norms
- Additional benefits may include:
- Health insurance
- Performance incentives
- Career growth in pharmacovigilance
- Exposure to global safety projects
Selection Process
The hiring process may include:
- Resume screening
- HR discussion
- Technical/medical interview
- Final round
How to Apply
Interested candidates should apply through the official Cencora careers portal.
- Ensure your resume highlights medical review and pharmacovigilance experience
- Include details of ICSR handling and regulatory exposure
Important Dates
- Last Date to Apply: July 30, 2026
- Early application is recommended
Why Apply for This Pharma Job?
This is a senior-level opportunity for medical professionals in drug safety. Key advantages include:
- Work on global pharmacovigilance and safety case processing
- Enhance expertise in ICSR review and regulatory compliance
- Collaborate with international healthcare and pharma clients
- Develop leadership and mentoring skills
- Strong career growth in drug safety and medical review
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with Cencora or any recruiter. We do not charge any fees for job applications. Candidates should verify all details from the official website before applying.
Final Call-to-Action
If you are an experienced MBBS professional in pharmacovigilance, this is your chance to step into a senior medical review role. Apply now and advance your career with Cencora.
