Pfizer Hiring Clinical Data Associate / Senior Associate – Freshers
- Pfizer Hiring Clinical Data Associate / Senior Associate – Freshers & Experienced | Mumbai Hybrid Clinical Data Jobs
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Data Management & Programming
- Clinical & Regulatory Compliance
- Collaboration & Reporting
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Skills Required
- Location & Salary
- Application Process
- Why This Role Matters in Healthcare
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this role?
- 2. Is this role open for freshers?
- 3. What skills are mandatory?
- 4. What is RBM in clinical trials?
- 5. What is the career growth?
- Summary Table
Pfizer Hiring Clinical Data Associate / Senior Associate – Freshers & Experienced | Mumbai Hybrid Clinical Data Jobs
Pfizer is hiring Clinical Data Associate / Senior Associate professionals for its Central Monitoring (RBM) team in Mumbai, Maharashtra. This is a hybrid, full-time opportunity open to freshers with relevant internships as well as experienced candidates in clinical data management, SAS programming, and clinical research analytics. With multiple applicants already showing interest, this role is ideal for candidates aiming to build or advance careers in clinical data science, risk-based monitoring (RBM), and pharmaceutical research.
Company Overview
Pfizer is one of the world’s leading biopharmaceutical companies, known for developing innovative medicines and vaccines that improve global health outcomes. With a strong presence in clinical research, data science, and drug development, Pfizer plays a critical role in advancing healthcare through cutting-edge research and regulatory excellence.
The company is globally recognized for its contributions to clinical trials, data-driven healthcare solutions, and regulatory compliance. Working at Pfizer provides exposure to advanced clinical data systems, global trial operations, and high-impact healthcare analytics projects.
Job Role & Responsibilities
As a Clinical Data Associate / Senior Associate in the Central Monitoring team, you will focus on analyzing clinical trial data, supporting RBM frameworks, and identifying risks using key risk indicators (KRIs). This role combines clinical knowledge with data analytics and programming expertise.
Core Responsibilities
- Perform centralized monitoring of clinical trial data to identify trends, risks, and inconsistencies
- Support Risk-Based Monitoring (RBM) activities using KRI-based assessments
- Analyze clinical datasets and generate insights for trial quality and compliance
- Assist in RBM system setup and configuration
Data Management & Programming
- Work with SAS programming for data analysis and reporting (mandatory skill)
- Utilize SQL / PL-SQL for querying clinical databases
- Support clinical data management (CDM) activities and database validations
- Collaborate with EDC and Oracle Clinical systems for data review and reporting
Clinical & Regulatory Compliance
- Ensure adherence to Good Clinical Practice (GCP) guidelines
- Maintain high standards of data quality and regulatory compliance
- Support clinical trial monitoring and reporting processes
Collaboration & Reporting
- Work independently as an Individual Contributor (IC role)
- Collaborate with cross-functional teams in clinical operations and data management
- Communicate findings effectively with stakeholders and project teams
Eligibility / Qualifications
Educational Qualification
Candidates must have a degree in Life Sciences or related disciplines.
Required courses include:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research
Experience
- Freshers with internship experience in SAS, clinical data, or programming can apply
- Experienced candidates with 2+ years in clinical data management, SAS programming, or research are preferred
Skills Required
- Strong knowledge of clinical trials and GCP guidelines
- SAS programming (mandatory)
- SQL / PL-SQL knowledge preferred
- Familiarity with EDC systems and Oracle Clinical
- Strong analytical and problem-solving skills
- Excellent communication skills and attention to detail
Location & Salary
- Job Location: Mumbai, Maharashtra, India
- Work Mode: Hybrid
n- Employment Type: Full-time - Salary: Competitive salary based on experience in clinical data management and analytics roles
Application Process
Interested candidates can apply through the official job posting link or contact directly:
Apply Here: https://www.linkedin.com/jobs/view/4395867407/
Email: sabita.roy@pfizer.com
Why This Role Matters in Healthcare
Clinical Data Associates play a critical role in ensuring the accuracy, integrity, and reliability of clinical trial data. By supporting centralized monitoring and risk-based approaches, this role contributes directly to faster drug approvals, improved trial quality, and safer healthcare outcomes for patients worldwide.
Frequently Asked Questions (FAQs)
1. Who can apply for this role?
Candidates with Life Sciences, Pharmacy, Biotechnology, or Clinical Research backgrounds can apply.
2. Is this role open for freshers?
Yes. Freshers with relevant internships in SAS or clinical data can apply.
3. What skills are mandatory?
SAS programming and understanding of clinical trials are mandatory.
4. What is RBM in clinical trials?
Risk-Based Monitoring (RBM) is a data-driven approach to monitor clinical trials using risk indicators.
5. What is the career growth?
You can grow into Clinical Data Scientist, RBM Specialist, SAS Programmer, or Clinical Research roles.
Summary Table
| Category | Details |
|---|---|
| Company | Pfizer |
| Vacancies | Clinical Data Associate / Senior Associate |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Biotechnology, Microbiology, Biochemistry, Life Sciences), Biomedical Sciences, Clinical Research |
| Experience | Freshers with Internship / 2+ Years Experience |
To apply for this job please visit www.linkedin.com.
