Apply for Pfizer Hiring Senior Associate Senior Central Monitor Chennai. Lead risk-based monitoring and ensure clinical trial data integrity.
About the Company
Pfizer is one of the world’s leading biopharmaceutical companies, driven by a mission to discover, develop, and deliver innovative medicines and vaccines that improve health and extend lives globally. With a strong legacy of scientific excellence and patient-centric innovation, Pfizer operates across the entire pharmaceutical value chain, from early research through clinical development and commercialization.Hiring Senior Associate Senior Central Monitor
The company is recognized for its robust clinical development capabilities, strong regulatory compliance culture, and commitment to data integrity. Pfizer embraces diversity, equity, and inclusion and provides equal employment opportunities across all regions in which it operates. Employees at Pfizer work in a collaborative, high-performing environment supported by advanced technologies and global expertise.
Joining Pfizer means contributing to high-impact clinical research programs while building a stable, long-term career in a globally respected organization. Hiring Senior Associate Senior Central Monitor
Job Details
- Job Title: Senior Associate, Senior Central Monitor
- Job Requisition ID: 4950342
- Job Type: Full Time
- Location: Chennai, India
- Work Model: Hybrid
- Job Category: Medical / Clinical Operations
This role is suited for experienced clinical research professionals with strong expertise in Risk-Based Monitoring (RBM), clinical data review, and centralized monitoring activities. Hiring Senior Associate Senior Central Monitor
Job Description
The Senior Central Monitor plays a critical role in ensuring the completeness, quality, and integrity of subject data in clinical trial databases under a Risk-Based Monitoring (RBM) model. The position focuses on proactive data surveillance, signal detection, and issue resolution to support effective oversight of clinical studies. Hiring Senior Associate Senior Central Monitor
This role involves developing and implementing RBM systems at the study level, defining and managing Key Risk Indicators (KRIs), and reviewing system outputs to identify signals and drive corrective actions. The Senior Central Monitor collaborates closely with global study teams, clinical data scientists, and other stakeholders to ensure monitoring activities comply with regulatory requirements, internal SOPs, and corporate standards.
The position requires strong technical expertise, independent decision-making, and the ability to support complex clinical trials across multiple phases. Hiring Senior Associate Senior Central Monitor
Key Responsibilities
General Responsibilities
- Implement global strategies, initiatives, and standardized processes to ensure high-quality, efficient, and consistent monitoring activities
- Ensure delivery of RBM activities in line with quality standards, timelines, and study deliverables
- Execute communication plans to maintain customer satisfaction and enable continuous improvements during study execution
- Provide technical expertise to influence stakeholders and resolve conflicts across global teams
System Setup Functions
- Set up and test study-level Risk-Based Monitoring systems to ensure system readiness and quality
- Define and configure Key Risk Indicators (KRIs) at the study level
- Ensure alignment between standard-level and study-level KRIs
- Confirm RBM system configuration aligns with study protocols, ICH-GCP, SOPs, corporate standards, and regulatory requirements
Hiring Senior Associate Senior Central Monitor
Data Review and Central Monitoring Functions
- Review RBM system outputs to identify signals and required actions
- Provide technical input to define issue resolution strategies for identified signals
- Perform centralized monitoring activities including signal detection, action proposal, and follow-up
- Collaborate with study teams to ensure timely resolution and mitigation of identified risks
- Work closely with Clinical Data Scientists to ensure signals and actions are appropriately managed and RBM systems released
Hiring Senior Associate Senior Central Monitor
Quality and Compliance
- Implement and maintain quality control documentation related to RBM activities
- Ensure data completeness, accuracy, and traceability
- Support audit readiness and regulatory compliance for RBM-related activities
Hiring Senior Associate Senior Central Monitor
Skills and Qualifications
Basic Qualifications
- Bachelor’s degree or higher in a scientific or business-related discipline, or equivalent experience
- Minimum of 4 years of experience in clinical trials (e.g., CRA, Data Management, Statistical Programming, or related roles)
- Technical expertise supporting clinical trial databases, data management, or site monitoring
- Strong understanding of clinical study management, data management, and regulatory operations
- Excellent verbal and written communication skills
- Ability to work independently with minimal supervision
- Strong organizational, time management, and multitasking abilities
- Experience working with internal and external stakeholders across global teams
Preferred Qualifications
- Strong understanding of the clinical development process across Phase I–IV trials
- Prior experience in clinical data management roles, including CRF design, database setup, edit checks, and data cleaning
- Knowledge of clinical trial databases and centralized monitoring tools
- Proficiency with Windows-based applications such as Word, Excel, PowerPoint, and Project
- Technical experience with Oracle, PL/SQL, SAS, Java, or relational database design
- Exposure to RBM models and centralized monitoring systems
Hiring Senior Associate Senior Central Monitor
Benefits and Perks
- Competitive salary aligned with global pharmaceutical industry standards
- Hybrid working model supporting flexibility and collaboration
- Opportunity to work on global, multi-phase clinical trials
- Exposure to advanced centralized monitoring and RBM technologies
- Professional development and career growth opportunities
- Inclusive and ethical work culture
- Strong focus on quality, compliance, and patient safety
Hiring Senior Associate Senior Central Monitor
Why You Should Join Pfizer
Pfizer offers a unique opportunity to work at the forefront of clinical research and data-driven decision-making. As a Senior Associate, Senior Central Monitor, you will directly contribute to safeguarding data integrity and patient safety through advanced risk-based monitoring approaches. Hiring Senior Associate Senior Central Monitor
This role allows you to work closely with global study teams, leverage cutting-edge RBM systems, and influence study outcomes across multiple therapeutic areas. Pfizer’s emphasis on quality, compliance, and innovation ensures that your work has meaningful impact on the development of medicines that reach patients worldwide.
If you are looking to advance your career in centralized monitoring and clinical operations within a globally respected organization, Pfizer provides the scale, support, and opportunity to succeed. Hiring Senior Associate Senior Central Monitor
FAQs
Is this a hybrid role?
Yes, this position follows a hybrid work model based in Chennai, India.
What experience is required for this role?
A minimum of 4 years of relevant clinical trial experience is required.
Does this role involve Risk-Based Monitoring?
Yes, RBM system setup, KRI management, and signal/action management are core responsibilities.
Will this role support regulatory inspections?
Yes, the role ensures RBM activities comply with regulatory standards and supports audit readiness.
Is programming experience mandatory?
Programming experience is preferred but not mandatory.
How to Apply
Interested candidates should apply through the official Pfizer careers portal by searching for Job Requisition ID 4950342 – Senior Associate, Senior Central Monitor. Complete the application with accurate professional and educational details to be considered.
Early applications are encouraged due to the strategic importance of this role.
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