GSK – Central Monitoring Lead | Bengaluru, India | Clinical Trials & RBQM
Company: GSK
Location: Bengaluru, India (Also Warsaw, Poland)
Job Type: Full-Time
Work Mode: Hybrid (2–3 days office)
Experience: 1–3+ Years (Central Monitoring / Clinical Research)
Qualification: Life Sciences / Pharmacy / Clinical Research or related field
Compensation:
Poland Salary Range: PLN 320,250 – PLN 533,750 annually (location-specific)
India Salary: Not disclosed (market competitive + bonus eligibility)
High-demand clinical research and centralized monitoring jobs are rapidly growing, especially roles focused on Risk-Based Monitoring (RBM), RBQM, and clinical data analytics.
SEO-friendly URL slug:
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Job Summary
GSK is hiring a Central Monitoring Lead to drive Risk-Based Quality Management (RBQM) and centralized monitoring strategies across global clinical trials. This role focuses on leveraging data analytics, risk management frameworks, and centralized monitoring tools to ensure high-quality, compliant, and efficient study delivery.
You will act as a subject matter expert (SME) in RBQM, Central Monitoring (CM), and Clinical Data Analytics, working closely with cross-functional teams including Clinical Operations, Biostatistics, Medical, and Safety.
This role is ideal for professionals aiming to grow in:
Clinical Trials & Clinical Operations
Central Monitoring & RBQM
Clinical Data Analytics
Risk Management in Drug Development
Key Responsibilities
RBQM & Central Monitoring Leadership
Lead implementation of Risk-Based Quality Management (RBQM) across studies
Oversee setup and execution of Centralized Monitoring (CM) and data analytics tools
Ensure compliance with ICH-GCP, regulatory requirements, and GSK SOPs
Clinical Data Analytics & Risk Management
Analyze study data to identify trends, signals, and potential risks
Interpret analytical signals and assess impact on trial execution
Drive mitigation strategies to prevent study failure
Study Oversight & Quality Assurance
Ensure monitoring plans include risk mitigation strategies:
Central Monitoring Plan
Monitoring Plan
Quality Tolerance Limit (QTL) Reports
Maintain high standards of data integrity, patient safety, and compliance
Cross-Functional Collaboration
Collaborate with:
Global Clinical Operations
Data Strategy & Management
Biostatistics & Programming
Medical & Safety Teams
Drive discussions on critical-to-quality factors
Vendor & Study Management
Oversee vendor deliverables and performance
Ensure consistent data quality oversight across multiple studies
Training & Mentorship
Act as SME for RBQM and Central Monitoring processes
Train and mentor team members using structured learning models (70-20-10)
Support capability building across global teams
Required Skills & Qualifications
1–3+ years of experience in Central Monitoring / Clinical Trials / Drug Development
Strong knowledge of:
Risk-Based Monitoring (RBM)
Risk-Based Quality Management (RBQM)
Clinical Data Analytics
Understanding of:
ICH-GCP guidelines
Clinical trial lifecycle (end-to-end)
Quality, safety, and compliance frameworks
Ability to interpret data visualizations and derive insights
Strong communication, influencing, and analytical skills
Experience with clinical data systems and monitoring tools
Preferred Skills (High SEO Keywords for Pharma Jobs):
Central Monitoring Tools (CMDA platforms)
Clinical Data Management (CDM)
Biostatistics & Statistical Programming basics
Signal Detection & Risk Assessment
Clinical Operations & Study Management
Data Visualization & Reporting
Perks & Benefits
Hybrid working model with flexible hours
Competitive salary with performance bonus eligibility
Medical insurance, life insurance, and retirement benefits
Exposure to global clinical trials and cutting-edge analytics tools
Career growth in clinical research leadership roles
Supportive and collaborative work environment
About the Company
GSK is a leading global biopharma company focused on vaccines, specialty medicines, and innovative therapies. With a mission to unite science, technology, and talent, GSK is driving advancements in clinical research and improving global health outcomes.
Why This Role is High-Impact
The Central Monitoring Lead role is one of the most strategic positions in modern clinical trials. With the industry shifting toward data-driven monitoring and decentralized trials, professionals skilled in RBQM and analytics are highly valued.
This role provides direct exposure to:
Advanced clinical trial analytics
Global regulatory frameworks
Risk-based monitoring strategies
Leadership in clinical operations
Career progression opportunities include:
Clinical Operations Lead
RBQM Specialist
Clinical Data Analytics Lead
Global Trial Manager
Application Process
Apply via GSK careers portal
Highlight experience with:
RBQM / RBM
Central Monitoring
Clinical Trials & GCP
Data Analytics & Visualization
Call to Action
If you want to step into a high-growth, high-impact clinical research leadership role, this is your opportunity.
Apply now and become a key driver of data-driven clinical trials and global drug development with GSK.
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