Looking to advance your career in clinical research, centralized monitoring, and RBQM (Risk-Based Quality Management)? GSK is hiring a Central Monitoring Lead for its Bengaluru location, offering a high-impact role in clinical trial data analytics and quality oversight.
This is an excellent opportunity for professionals with experience in centralized monitoring, data analytics, and clinical development, aiming to work with a global biopharma leader.
Job Overview
- Role: Central Monitoring Lead
- Company: GSK
- Location: Bengaluru, India (Hybrid)
- Employment Type: Full-Time
- Experience Required: 1โ3 years
- Application Deadline: April 8, 2026
Key Responsibilities โ Central Monitoring Lead
As a Central Monitoring Lead, you will:
- Lead implementation of Risk-Based Quality Management (RBQM) across clinical studies
- Set up and execute Centralized Monitoring (CM) and Data Analytics (DA) strategies
- Collaborate with Clinical Operations, Data Management, Stats, Medical & Safety teams
- Identify critical-to-quality (CtQ) risks and develop mitigation strategies
- Analyze clinical trial data signals and trends for risk detection
- Ensure compliance with ICH-GCP, SOPs, and regulatory requirements
- Manage study-level data analytics investigations and vendor performance
- Train and mentor teams on RBQM tools and centralized monitoring processes
Required Qualifications
To apply for this Central Monitoring Lead job, candidates must have:
- 1โ3 years of experience in centralized monitoring in clinical trials
- Strong knowledge of RBQM tools and clinical data analytics
- Understanding of ICH-GCP, compliance, and risk management principles
- Experience in end-to-end clinical development lifecycle
- Ability to interpret data visualizations and analytics insights
- Excellent communication, analytical, and influencing skills
- Fluent English (written and spoken)
Preferred Skills
- Expertise in clinical trial data review and signal detection
- Familiarity with central monitoring plans and QTL reporting
- Experience working with global CRO/pharma teams
Benefits of Working at GSK
- Hybrid working model (2โ3 days office)
- Flexible work hours
- Global exposure in a leading biopharma company
- Medical insurance, life insurance, and retirement benefits
- Performance-based bonuses
- Career growth in clinical data analytics & RBQM domain
- Collaborative and supportive work environment
Why This Role is High-Value
This role is critical in modern clinical trial transformation, where companies are shifting from traditional monitoring to risk-based and data-driven monitoring approaches. You will directly contribute to:
- Improving data integrity and patient safety
- Reducing clinical trial risks and delays
- Enhancing regulatory compliance and audit readiness
How to Apply
