Pfizer, a global leader in biopharmaceutical innovation, is hiring a Senior Associate – Senior Central Monitor for its India operations in Chennai. This opportunity is ideal for professionals with strong experience in clinical trial monitoring, Risk-Based Monitoring (RBM), data management, and central monitoring activities.
The Senior Central Monitor job at Pfizer plays a critical role in ensuring data quality, integrity, and compliance across clinical trials while working closely with global study teams under the RBM framework.
If you are seeking a central monitoring job in clinical research with a reputed multinational organization, this role offers excellent exposure, career growth, and a hybrid work model.
Key Responsibilities – Senior Central Monitor (RBM)
General Responsibilities
- Implement global RBM strategies, processes, and quality standards
- Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
- Collaborate with global stakeholders to meet study timelines and objectives
- Provide technical expertise and customer-focused communication
RBM System Setup
- Configure and test study-level Risk-Based Monitoring systems
- Define and manage Key Risk Indicators (KRIs)
- Ensure RBM systems align with study protocols and regulatory standards
Central Data Review & Monitoring
- Review RBM system outputs for signal and action management
- Perform centralized monitoring to ensure data completeness and accuracy
- Support issue resolution and follow up with study teams
- Maintain quality control documentation for RBM activities
- Partner with Clinical Data Scientists to mitigate risks and release RBM systems
Eligibility Criteria & Qualifications
Required Qualifications
- Bachelor’s degree or higher in Life Sciences, Pharmacy, Clinical Research, or related discipline
- Minimum 4 years of experience in clinical trials (CRA, Data Management, Programmer, Central Monitor, etc.)
- Strong understanding of clinical trial data, monitoring, and regulatory processes
- Excellent verbal and written communication skills
- Ability to work independently and manage multiple priorities
Preferred Qualifications
- Knowledge of Phase I–IV clinical development and study design principles
- Prior experience in clinical data management, CRF design, database setup, and data cleaning
- Familiarity with clinical trial databases and RBM tools
- Technical skills in Oracle, PL/SQL, SAS, Java, or relational databases
- Proficiency in MS Office tools (Excel, Word, PowerPoint, Project)
Why Join Pfizer? – Benefits & Work Culture
- Global exposure with world-class clinical research projects
- Hybrid work model for better work-life balance
- Competitive salary and performance-based growth
- Strong focus on compliance, ethics, and employee development
- Inclusive workplace with equal opportunity employment
Salary Package (Estimated)
💰 ₹12,00,000 – ₹18,00,000 per annum (CTC)
(Salary may vary based on experience, skills, and internal policies)
How to Apply
