Pfizer is hiring for an Associate Database Analyst, Clinical Database Management position in Chennai, India. The opportunity is a full-time hybrid role within Pfizer’s clinical development organization and focuses on clinical data monitoring, database quality, documentation, validation, and clinical data management activities.
According to the current Pfizer job listing, the position requires a BA/BS degree with any years of experience and knowledge of ICH/GCP documentation requirements, clinical development processes, regulatory requirements, and electronic data/document management systems. Pfizer
This role can be relevant for candidates interested in clinical data management, clinical database management, clinical research, CTMS, data validation, and pharmaceutical operations.
Job Details
| Category | Details |
|---|---|
| Company | Pfizer |
| Job Title | Associate Database Analyst, Clinical Database Management |
| Job ID | 4964296 |
| Location | Chennai, India |
| Work Model | Hybrid |
| Employment Type | Full Time |
| Experience | Any years of experience |
| Qualification | BA/BS |
| Job Area | Clinical Database Management |
Pfizer’s careers platform currently lists Chennai among its India locations and identifies multiple current full-time opportunities there. Pfizer
What Does an Associate Database Analyst Do?
The Associate Database Analyst will support activities related to the quality and management of clinical trial data. The position involves reviewing clinical data, managing queries, investigating logic-check flags, and supporting the testing and validation of clinical data collection systems.
The role also involves collaboration with study teams and stakeholders responsible for clinical documentation and Trial Master File activities.
Key Responsibilities
- Perform Data Monitoring and Management (DMM) activities, including data review and query management.
- Investigate logic-check flags and support resolution of data issues.
- Support the design, documentation, testing, validation, and implementation of clinical data collection tools and systems.
- Act as a first point of contact for Clinical Trial Management System (CTMS) questions and issues.
- Follow applicable SOPs and working practices.
- Work with Study Team Points of Contact, Document Owners, and TMF Study Owners to resolve documentation discrepancies.
- Contribute to process improvement initiatives and additional clinical data management projects.
- Support the accuracy, integrity, and consistency of clinical data.
Eligibility Criteria
Candidates must have:
- BA/BS degree in a relevant discipline.
- Knowledge of ICH/GCP documentation requirements.
- Experience with electronic documentation management systems and/or web-based data management systems.
- Awareness of the clinical development process.
- Strong understanding of Good Clinical Practice (GCP) principles.
- Knowledge of regulatory requirements and relevant data standards.
- Strong written and verbal English communication skills.
- Proficiency in Microsoft Office Suite.
Preferred Qualifications
Pfizer also lists the following as preferred:
- Experience with Clinical Trial Management Systems (CTMS).
- Familiarity with data validation and quality-control processes.
- Strong collaboration and problem-solving skills.
- High attention to detail.
- Experience with AI tools such as ChatGPT or Microsoft Copilot for productivity and problem solving.
- Understanding of responsible AI practices, including risk management and ethical use.
Skills Required
Clinical Data Management | Clinical Database Management | CTMS | Data Validation | Data Monitoring | Query Management | ICH-GCP | Clinical Research | Data Quality | Regulatory Requirements | TMF Documentation | Microsoft Office | Problem Solving
Who Can Apply?
This Pfizer Associate Database Analyst opportunity is suitable for graduates who meet the BA/BS requirement and are interested in clinical data and pharmaceutical research operations.
Candidates with exposure to clinical research, clinical data management, CTMS, electronic documentation systems, GCP, data validation, or healthcare data may find the role particularly relevant.
Benefits and Career Exposure
The job description identifies several areas of professional exposure rather than specifying a detailed employee-benefits package:
- Hybrid work arrangement
- Exposure to clinical development and clinical data management
- Experience with clinical data monitoring and validation
- Collaboration with cross-functional clinical study teams
- Exposure to CTMS and electronic data-management systems
- Experience with ICH/GCP and regulatory requirements
- Opportunity to work with modern generative AI tools in a responsible manner
The position also provides exposure to clinical database activities that support the quality and timely delivery of clinical data.
How to Apply
