Pfizer has announced an exciting opportunity for Associate Data Manager professionals in Chennai. Candidates having 1-3 years of Clinical Data Management (CDM) experience and a Life Sciences background can apply for this hybrid position.
This opportunity is ideal for professionals looking to build their careers in Clinical Data Management, Clinical Trials, CTMS, Data Review, Query Management, ICH-GCP Compliance, and Electronic Data Capture (EDC) while working with one of the world’s leading pharmaceutical companies.
If you are searching for Pfizer Associate Data Manager Jobs 2026, Clinical Data Management Jobs in Chennai, Hybrid Pharma Jobs, or CDM Jobs in India, this opening offers an excellent opportunity to work on global clinical development projects.
Job Details
| Particular | Details |
|---|---|
| Company | Pfizer |
| Job Title | Associate Data Manager |
| Location | Chennai, Tamil Nadu |
| Work Mode | Hybrid |
| Experience | 1โ3 Years |
| Qualification | Bachelor’s Degree in Life Sciences |
| Department | Clinical Data Management |
| Industry | Pharmaceutical / Clinical Research |
Key Responsibilities
The selected Associate Data Manager will be responsible for:
- Support completion of clinical project milestones within defined timelines.
- Participate in Data Monitoring and Management (DMM) activities.
- Perform clinical data review and query management.
- Ensure high-quality database design, documentation, validation, testing, and implementation.
- Support Clinical Trial Management System (CTMS) users as the first point of contact.
- Follow Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP).
- Investigate logic check flags and resolve discrepancies.
- Coordinate with Study Teams, TMF Owners, Document Owners, and cross-functional stakeholders.
- Identify and resolve documentation-related issues.
- Contribute to process improvements and operational excellence initiatives.
- Support additional clinical data management projects as required.
Required Qualifications
Applicants should possess:
- Bachelor’s Degree in Life Sciences
- 1โ2 years of Clinical Data Management experience
- Knowledge of ICH-GCP documentation requirements
- Experience with Electronic Documentation Management Systems
- Exposure to web-based Clinical Data Management systems
- Understanding of the clinical development lifecycle
- Familiarity with regulatory requirements and clinical data standards
- Excellent analytical and attention-to-detail skills
- Strong written and verbal English communication
- Proficiency in Microsoft Office Suite
Preferred Qualifications
Candidates with the following experience will have an advantage:
- Management of medical and clinical study documentation
- Trial Master File (TMF) documentation
- CTMS support
- Electronic Clinical Documentation Management
- Clinical records management
Why Join Pfizer?
Working at Pfizer provides professionals with opportunities to:
- Build expertise in global Clinical Data Management
- Work in a hybrid environment
- Gain exposure to international clinical trials
- Collaborate with experienced global study teams
- Enhance knowledge of CTMS, TMF, and regulatory compliance
- Develop long-term career growth within one of the world’s leading pharmaceutical companies
Skills Required
- Clinical Data Management
- Data Review
- Query Management
- CTMS
- TMF
- Clinical Trial Documentation
- ICH-GCP
- SOP Compliance
- Regulatory Documentation
- Microsoft Office
- Communication Skills
- Attention to Detail
Location
Chennai, Tamil Nadu (Hybrid Work Model)
Candidates willing to relocate are encouraged to apply.
How to Apply
Interested candidates can share their updated resume through the following contact details:
Email: Tejaswini.Desai@pfizer.com
Applicants are encouraged to apply as early as possible.
