Manager Drug Safety Physician Job at Cencora Noida. MBBS and MD candidates can grow in pharmacovigilance leadership roles globally.
Are you a qualified medical professional with experience in pharmacovigilance and drug safety? Cencora is offering an excellent leadership opportunity for the role of Manager – Drug Safety Physician in Noida. This position is ideal for MBBS/MD professionals who want to work on aggregate safety reports, benefit-risk evaluation, and global regulatory submissions within a reputed healthcare organization.
Company Overview
Cencora is a global pharmaceutical services and healthcare solutions company committed to improving patient outcomes. Through its affiliate PharmaLex India Private Limited, the organization delivers high-quality services in pharmacovigilance, regulatory affairs, and compliance. Cencora operates across multiple international markets, supporting drug safety and lifecycle management for pharmaceutical companies.
Job Overview
| Job Title | Manager – Drug Safety Physician |
|---|---|
| Company | Cencora (PharmaLex India Pvt. Ltd.) |
| Location | Noida, Uttar Pradesh, India |
| Employment Type | Full-Time |
| Department | Pharmacovigilance / Drug Safety |
| Experience | 5–7 Years |
| Qualification | MBBS / MD |
| Application Mode | Online Application |
| Job Requisition ID | R264402 |
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 Drug Safety and Pharmacovigilance team, focusing on aggregate report writing, medical review, and regulatory compliance. The position involves collaboration with global teams and health authorities for safety data evaluation.
Key Roles & Responsibilities
As a Manager – Drug Safety Physician, you will lead safety report preparation and ensure regulatory compliance across global markets.
Safety Report Writing & Management
- Developing and managing aggregate safety reports, including:
- PSUR / PBRER
- Risk Management Plans (RMP)
- DSURs and ACOs
- Ensuring reports are high-quality, medically accurate, and regulatory compliant
- Managing timelines, tracking commitments, and coordinating report submissions
Medical Review & Safety Evaluation
- Performing medical review of safety data, including:
- Clinical trial data
- Safety databases
- Literature and epidemiology data
- Conducting benefit-risk assessments and safety evaluations
- Addressing queries from regulatory authorities
Regulatory Compliance & Coordination
- Ensuring alignment with global regulatory requirements
- Updating RMPs based on health authority feedback
- Coordinating with cross-functional teams to gather required data
- Managing annexes and supporting documents for submissions
Leadership & Team Management
- Mentoring and guiding pharmacovigilance team members
- Reviewing and ensuring quality of safety documents
- Conducting training sessions and knowledge sharing
- Supporting team performance and development
Stakeholder & Communication Management
- Interacting with clients and regulatory authorities
- Addressing stakeholder comments and feedback
- Preparing responses to regulatory queries
- Supporting project coordination and communication
Quality & Process Management
- Performing peer reviews and quality checks
- Maintaining documentation as per SOPs and regulatory standards
- Ensuring consistency across all safety reports
- Driving continuous improvement in safety processes
Eligibility Criteria
Educational Qualification
Candidates must have:
- MBBS (Bachelor of Medicine, Bachelor of Surgery)
- MD (Doctor of Medicine) (preferred)
Experience Required
- Minimum 5 to 7 years of experience in:
- Pharmacovigilance
- Drug safety
- Medical review
- Experience in:
- Aggregate safety reports (PSUR, RMP, DSUR)
- ICSR processing and signal detection
- Regulatory submissions
Skills Required
- Strong clinical judgment and analytical skills
- In-depth knowledge of pharmacovigilance processes
- Expertise in global regulatory guidelines and GxP
- Excellent communication and presentation skills
- Leadership and mentoring capabilities
- Strong organizational and problem-solving skills
- Ability to work under pressure and meet deadlines
- Familiarity with safety databases and literature review
Salary & Benefits
- Salary will be as per company norms
- Additional benefits may include:
- Health and insurance coverage
- Performance incentives
- Leadership development programs
- Exposure to global pharmacovigilance operations
Selection Process
The hiring process may include:
- Resume screening
- HR discussion
- Technical/medical interview
- Final leadership round
How to Apply
Interested candidates should apply through the official Cencora careers portal.
- Ensure your resume highlights safety report writing and medical review experience
- Include regulatory exposure and leadership experience
Important Dates
- No fixed deadline mentioned
- Early application is recommended
Why Apply for This Pharma Job?
This role offers a senior-level opportunity for medical professionals in pharmacovigilance. Key benefits include:
- Work on global drug safety and regulatory reporting
- Lead preparation of critical safety documents
- Collaborate with international regulatory authorities
- Develop leadership skills in pharmacovigilance
- Career growth into senior medical and safety roles
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with Cencora or any employer. We do not charge any fees for job applications. Candidates should verify all job details from the official website before applying.
Final Call-to-Action
If you are an MBBS or MD professional with pharmacovigilance experience, this is your chance to step into a leadership role. Apply now and advance your career in drug safety with Cencora.
