Pfizer is hiring professionals for its Central Monitoring Team for the position of Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences. The role focuses on Risk-Based Monitoring (RBM), clinical trial data surveillance, data quality assessment, and risk indicator management.
Candidates with 1+ years of experience in SAS and/or SQL programming and educational backgrounds in pharmacy, life sciences, statistics, or technology can consider this opportunity. The work arrangement is hybrid, with locations listed as Chennai and Mumbai in the recruitment announcement.
Pfizer Job Details
| Job Detail | Information |
|---|---|
| Company | Pfizer |
| Position | Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences |
| Department | Central Monitoring Team |
| Job Locations | Chennai and Mumbai |
| Work Type | Full-time, Hybrid |
| Experience | 1+ years in SAS and/or SQL programming |
| Job Requisition ID | 4964498 |
About the Role
The Senior Associate, Central Monitor supports clinical trial data quality and integrity through Risk-Based Monitoring. The role involves configuring and testing RBM systems, reviewing monitoring outputs, defining key risk indicators (KRIs), and coordinating the resolution of identified issues with global study teams.
The position also involves quality oversight, data quality assessment, and compliance with clinical research standards and applicable regulatory requirements.
Eligibility Criteria
Required experience: 1+ years of experience in SAS and/or SQL programming.
Relevant educational backgrounds:
- B.Pharm
- M.Pharm
- Pharm.D
- M.Sc.
- B.Sc.
- Life Sciences
- Statistics
- Technology-related backgrounds
Key Responsibilities
- Set up and test study-level Risk-Based Monitoring systems.
- Define and configure Key Risk Indicators (KRIs).
- Configure Data Quality Assessment (DQA) dictionaries.
- Review clinical trial protocols and RBM system outputs.
- Support signal identification, action management, and issue resolution.
- Ensure clinical trial monitoring activities follow ICH GCP, SOPs, corporate standards, and regulatory requirements.
- Implement quality control procedures and maintain RBM documentation.
- Coordinate with Clinical Data Scientists and global study teams.
- Document lessons learned and support continuous process improvement.
Required Skills
- SAS and/or SQL programming
- Risk-Based Monitoring (RBM)
- Clinical trial data surveillance
- Key Risk Indicators (KRIs)
- Data Quality Assessment (DQA)
- Clinical data quality and integrity
- Signal and action management
- ICH GCP and SOP compliance
- Technical troubleshooting and stakeholder communication
