Pfizer Hiring for Clinical Data Management & Pharmacovigilance - Chennai & Mumbai
Are you seeking high-paying Pfizer Careers in India, Clinical Data Management Jobs, or Pharmacovigilance Careers? Global biopharmaceutical leader Pfizer has announced recruitment for two experienced roles: **Senior Associate – Aggregate Report Analyst** in Chennai and **Senior Associate, Data Manager – Clinical Data Sciences** in Mumbai. Both positions offer hybrid working arrangements and competitive salary structures.
These roles are suitable for pharmacy, clinical research, biotechnology, or life sciences professionals with 2 or more years of experience in drug safety, aggregate safety reporting (PSUR/PBRER), and electronic data capture (EDC) systems. To learn how to apply successfully, read our guide on how to apply for healthcare and pharma jobs online.
📋 Job Openings & Details
| Particulars | Job 1: Aggregate Report Analyst | Job 2: Clinical Data Sciences Data Manager |
|---|---|---|
| Position | Senior Associate – Aggregate Report Analyst | Senior Associate, Data Manager – Clinical Data Sciences |
| Company | Pfizer | Pfizer |
| Location | Chennai, India (Hybrid) | Mumbai, India (Hybrid) |
| Employment Type | Full-Time | Full-Time |
| Experience Required | 2 Years+ in PV / Drug Safety | 2 Years+ in Clinical Data Management |
| Qualifications | Bachelor's/Master's/PharmD/PhD in Life Sciences, Pharmacy, or Medicine | BA/BS/MS/MBA in Life Sciences or related field |
| Estimated Salary | ₹12,00,000 – ₹20,00,000 per annum | ₹11,00,000 – ₹18,00,000 per annum |
| Application Deadline | Apply Immediately (Not Mentioned) | Apply Immediately (Not Mentioned) |
💼 Job 1: Senior Associate – Aggregate Report Analyst (Chennai)
The selected candidate supports the Worldwide Safety department by preparing high-quality aggregate safety reports and benefit-risk assessments that meet global regulatory compliance standards.
Key Responsibilities
- Prepare and author critical regulatory safety reports, including Development Safety Update Reports (DSUR), Periodic Safety Update Reports (PSUR), Periodic Benefit-Risk Evaluation Reports (PBRER), and Risk Management Plans (RMP).
- Support Addendum Clinical Overviews (ACO) and perform integrated safety data analyses.
- Collaborate actively with Regulatory Affairs, Clinical, Medical, Epidemiology, and QPPV global teams.
- Coordinate and drive document strategy, timeline compliance, and benefit-risk messaging.
- Ensure complete compliance with FDA, EMA, ICH guidelines, and internal safety SOPs.
Preparing aggregate safety reports requires a deep understanding of drug safety principles. Test your skills with our comprehensive Top 100 Entry Level Pharmacovigilance Questions.
💼 Job 2: Senior Associate, Data Manager – Clinical Data Sciences (Mumbai)
The selected candidate oversees clinical data management activities, ensuring high-quality, compliant data to support global regulatory submissions and clinical trials.
Key Responsibilities
- Manage clinical trial Data Monitoring and Management (DMM) activities and completeness reviews.
- Develop, update, and review data cleaning reports and Data Management Plans (DMPs).
- Utilize web-based Clinical Data Management Systems and Electronic Data Capture (EDC) platforms.
- Work with global cross-functional teams, documenting study learnings and best operational practices.
- Ensure compliance with CDISC standards, ICH-GCP, and global regulatory rules.
Clinical data manager workflows require a clear understanding of database coordination and analytics. To check how clinical data coordinator and manager pathways compare with clinical programming, read our detailed comparison on Clinical SAS vs Clinical Data Management.
🎓 Qualifications & Experience Requirements
Candidates applying for these senior associate positions should meet the following qualifications:
- Degrees: B.Pharm, M.Pharm, PharmD, BSc or MSc in Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Pharmaceutical Sciences, or Medicine (preferred for senior roles).
- Experience: Minimum 2 years of relevant experience in Pharmacovigilance / Drug Safety (for Chennai role) or Clinical Data Management (for Mumbai role).
- Familiarity with EDC, CDISC standards, and safety reporting regulations (FDA / EMA).
For pharmacy graduates planning their career paths and evaluating global salary scales, check our guide on B.Pharm Career: India vs USA.
Required Core Skills
- Expertise in Pharmacovigilance operations and Aggregate Reporting (DSUR/PSUR/PBRER/RMP).
- Knowledge of Clinical Trial operations, clinical data review, and EDC Systems.
- High level of compliance with ICH-GCP, FDA, and EMA guidelines.
- Strong scientific writing, data analysis, and benefit-risk assessment capabilities.
- Familiarity with data visualization tools and AI tools (such as ChatGPT or Copilot) is a plus.
💰 Salary & Employee Benefits
- Aggregate Report Analyst: ₹12,00,000 – ₹20,00,000 per annum (Estimated).
- Clinical Data Sciences Data Manager: ₹11,00,000 – ₹18,00,000 per annum (Estimated).
- Hybrid working model providing flexibility and work-life balance.
- Exposure to international projects, collaborating with global teams across the US and Europe.
- Comprehensive medical insurance and professional training programs.
To see how pharmacovigilance and data management compensation scales between India and US markets, check our analysis on Pharmacovigilance Salary: India vs USA.
🌟 Why Join Pfizer?
- Pfizer is one of the world's most recognized biopharmaceutical companies, dedicated to discovering and developing life-changing medicines.
- Collaborative and diverse workplace culture that emphasizes patient safety and professional development.
- Excellent launchpad for mid-level professionals to step into global leadership roles.
📑 Resume Tips for Pfizer Vacancies
- Highlight your specific number of years of experience in Aggregate Safety Reporting or Clinical Data Management.
- List any clinical trial management systems, EDC databases, or regulatory standards (e.g. CDISC SDTM) you have worked with.
- Keep your resume clean, well-structured, and optimized for applicant tracking systems (ATS).
🎯 Pfizer Senior Associate Interview Questions
- What are the core differences between a Development Safety Update Report (DSUR) and a Periodic Safety Update Report (PSUR)?
- How do you construct and test data cleaning edit checks in an EDC system?
- What is a Risk Management Plan (RMP), and what are its key modules?
- Describe your experience with CDISC data standards. How do they streamline regulatory operations?
- How do you manage deadlines and prioritize data reviews across multiple global clinical sites?
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Pfizer's official Workday job board. Use the corresponding links below for your desired position. Since no specific application deadline is mentioned, candidates are advised to apply immediately. For step-by-step guidance on setting up your application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
❓ Frequently Asked Questions
Q. What is the application deadline?
No deadline is mentioned in the official post. Candidates are advised to apply immediately.
Q. Who is eligible to apply?
Candidates with B.Pharm, M.Pharm, PharmD, or B.Sc/M.Sc in Life Sciences, Biotechnology, Microbiology, or related fields (2+ years experience).
Q. Where are these positions based?
The Aggregate Report Analyst position is based in Chennai, and the Data Manager position is based in Mumbai (both hybrid work models).
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