GlaxoSmithKline (GSK), a global biopharmaceutical leader, is hiring for Central Monitor and Study Manager roles to strengthen its global clinical operations and Risk Based Quality Management (RBQM) framework. These opportunities are ideal for professionals with experience in clinical trials, centralized monitoring, data review, and study management, looking to grow their careers in a high-impact, international environment.
These roles offer exposure to global clinical studies, advanced data analytics, and cross-functional collaboration, supporting GSK’s mission to unite science, technology, and talent to get ahead of disease together.
🧪 Open Positions at GSK
1️⃣ Central Monitor – Clinical Research
Key Responsibilities
- Perform centralized monitoring activities from study start to database lock
- Review clinical study data to identify trends, risks, and quality issues
- Use analytics tools to support Risk Based Monitoring (RBM)
- Communicate findings and risk mitigation actions to study teams
- Maintain inspection-ready documentation and monitoring records
- Train study teams on RBQM and centralized monitoring processes
Required Qualifications
- Bachelor’s degree in Life Sciences, Health, Statistics, or related field
- Minimum 3 years’ experience in clinical trials or clinical operations
- Experience in centralized data review or clinical data monitoring
- Strong knowledge of ICH-GCP and global clinical regulations
- Excellent English communication skills
Preferred Skills
- Experience with Spotfire, CluePoints, or similar tools
- Knowledge of RBM and RBQM frameworks
- Basic data skills (SQL, R, Python)
- Experience working with global teams
2️⃣ Study Manager – Clinical Operations
Key Responsibilities
- Lead and coordinate clinical studies from planning to close-out
- Monitor study timelines, risks, budgets, and quality metrics
- Draft and review protocols, ICFs, and study plans
- Oversee CROs, vendors, and country-level study execution
- Ensure eTMF completeness and inspection readiness
- Manage study budgets, invoices, and change orders
- Support clinical supply and investigational product delivery
Required Qualifications
- 3+ years’ experience in clinical research or pharma environment
- Strong knowledge of clinical trial conduct and drug development
- In-depth understanding of ICH-GCP and regulatory requirements
- Experience with Trial Master File (TMF) systems
- Strong project management and stakeholder coordination skills
🎯 Why Join GSK?
Employee Benefits
- Hybrid working model (2–3 days office/week)
- Flexible working hours
- Competitive salary with annual performance bonus
- Medical insurance, life insurance & retirement benefits
- International exposure and structured career growth
- Inclusive, collaborative, and patient-focused work culture
💰 Estimated Salary (India – Bengaluru)
- Central Monitor: ₹18 – ₹30 LPA
- Study Manager: ₹15 – ₹25 LPA
(Actual compensation may vary based on experience, role scope, and internal equity.)
📝 How to Apply
Application Link for Central Monitor
Application Link for Study Manager
