Pfizer has announced exciting career opportunities for experienced life sciences professionals in India. The company is currently hiring for Senior Associate โ Aggregate Report Analyst in Chennai and Senior Associate, Data Manager โ Clinical Data Sciences in Mumbai.
These Pfizer jobs are ideal for candidates with backgrounds in pharmacovigilance, clinical research, regulatory affairs, clinical data management, and drug safety. Professionals with experience in ICH-GCP, clinical trials, aggregate reporting, risk management, or electronic data capture (EDC) systems are encouraged to apply.
If you’re looking for Pfizer jobs in India, clinical data management jobs, pharmacovigilance jobs, or drug safety careers, these opportunities offer global exposure, hybrid work, and excellent career progression.
Job 1: Senior Associate โ Aggregate Report Analyst
Company: Pfizer
Location: Chennai, India
Employment Type: Full-Time
Work Mode: Hybrid
Job Overview
The Senior Associate โ Aggregate Report Analyst supports the Worldwide Safety department by preparing high-quality aggregate safety reports and benefit-risk assessments that meet global regulatory requirements. The role collaborates with cross-functional teams across Europe, the United States, and Asia to ensure regulatory compliance and patient safety.
Key Responsibilities
- Prepare aggregate safety reports including:
- Development Safety Update Reports (DSUR)
- Periodic Safety Update Reports (PSUR)
- Periodic Benefit-Risk Evaluation Reports (PBRER)
- Risk Management Plans (RMP)
- Addendum Clinical Overviews (ACO)
- Perform integrated safety data analyses.
- Support responses to regulatory safety queries.
- Collaborate with Regulatory Affairs, Clinical, Medical, Epidemiology, QPPV, and Global Safety teams.
- Ensure compliance with ICH, FDA, EMA, and internal SOPs.
- Drive document strategy and benefit-risk messaging.
- Coordinate timelines and deliver regulatory documents within deadlines.
- Support process improvements and quality initiatives.
- Review contractor or co-author contributions when required.
Eligibility
- Bachelor’s degree in Life Sciences.
- Minimum 2 years of experience in:
- Pharmacovigilance
- Drug Safety
- Clinical Research
- Regulatory Affairs
- Clinical Development
- Strong scientific writing skills.
- Knowledge of ICH Guidelines, FDA, EMA regulations.
- Excellent analytical and communication skills.
Preferred Qualifications
- PharmD, MD, DVM, Master’s or PhD.
- Experience with Microsoft Office tools.
- Knowledge of statistics and epidemiology.
- Prior aggregate reporting experience is highly desirable.
Job 2: Senior Associate, Data Manager โ Clinical Data Sciences
Company: Pfizer
Location: Mumbai, India
Employment Type: Full-Time
Work Mode: Hybrid
Job Overview
The Clinical Data Sciences team is seeking an experienced Data Manager to oversee data management activities for clinical trials while ensuring high-quality, compliant clinical data that supports regulatory submissions and medical decision-making.
Key Responsibilities
- Manage clinical trial Data Monitoring and Management (DMM).
- Maintain data quality and completeness.
- Develop and review data cleaning reports.
- Support Data Management Plans.
- Work with global cross-functional teams.
- Document study learnings and best practices.
- Utilize web-based clinical data management systems.
- Ensure compliance with ICH-GCP and regulatory standards.
Eligibility
- BA/BS with 2+ years of experience OR MBA/MS.
- Experience in Clinical Data Management.
- Knowledge of:
- Electronic Data Capture (EDC)
- Clinical Data Management Systems
- Electronic Document Management Systems
- Clinical Trial Management
- Regulatory Operations
- Strong communication and analytical skills.
Preferred Qualifications
- Master’s degree.
- Pharmaceutical industry experience.
- Experience with data visualization tools.
- Knowledge of AI tools including ChatGPT or Microsoft Copilot.
- Understanding of CDISC and regulatory data standards.
Why Join Pfizer?
Working at Pfizer provides employees with opportunities to contribute to global healthcare innovation while collaborating with international experts.
Benefits
- Hybrid working model
- Global career opportunities
- International project exposure
- Learning and development programs
- Cross-functional collaboration
- Competitive salary and benefits
- Inclusive workplace culture
- Career growth in pharmacovigilance and clinical research
Who Should Apply?
These positions are suitable for professionals from:
- B.Pharm
- M.Pharm
- PharmD
- BSc Life Sciences
- MSc Life Sciences
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Pharmaceutical Sciences
- Medicine (Preferred for senior roles)
Skills Required
- Pharmacovigilance
- Aggregate Reporting
- Clinical Data Management
- Drug Safety
- Clinical Trials
- ICH-GCP
- Regulatory Affairs
- FDA Guidelines
- EMA Regulations
- Risk Management Plans
- DSUR
- PSUR
- PBRER
- Clinical Data Review
- EDC Systems
- Microsoft Excel
- Scientific Writing
- Data Analysis
- Benefit-Risk Assessment
Salary (Estimated)
Based on current market benchmarks in India:
Senior Associate โ Aggregate Report Analyst
โน12,00,000 โ โน20,00,000 per annum
Senior Associate โ Data Manager, Clinical Data Sciences
โน11,00,000 โ โน18,00,000 per annum
Actual compensation depends on experience, qualifications, and internal compensation policies.
How to Apply
Application Link For Senior Associate โ Aggregate Report Analyst
Application Link For Senior Associate โ Data Manager, Clinical Data Sciences
