Central Monitor (Bengaluru)

Central Monitor (Bengaluru)

09 Sep
|
GSK
|
Bengaluru

09 Sep

GSK

Bengaluru

Site Name: Warsaw, Bengaluru Luxor North Tower
Posted Date: Jan 27 2026

You will join the Central Monitoring team in Poland to support Risk Based Quality Management across global clinical studies. You will review study data centrally, use data analytics to find trends and risks, and work with study teams to reduce those risks. We value curious problem-solvers who communicate clearly, learn quickly, and act with care for patients and data quality. This role offers strong learning and growth opportunities and the chance to make a measurable impact by improving how clinical research protects participants and delivers reliable results. You will help unite science, technology and talent to get ahead of disease together.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Perform centralized monitoring of study data from study start through database lock, following the study monitoring plan.
- Use data analytics tools to identify trends, data quality issues, and risks at site, country, and study levels.




- Communicate findings and recommended actions to study teams and support timely issue resolution and escalation.
- Maintain documentation and achieving central monitoring reviews and ensure inspection readiness.
- Support setup and ongoing maintenance of data analytics tools used for centralized monitoring.
- Train and coach central and local study teams on central monitoring processes and Risk Based Quality Management principles.

Why You?

Working model

This role is hybrid. You will be expected to work from the office on a regular cadence and work remotely as agreed with your manager.

Basic Qualification

We are seeking professionals with the following required skills and qualifications to help us achieve our goals
- Bachelor’s degree in life science, health, statistics, or related discipline.
- Minimum 3 years’ experience in clinical trials, clinical operations, or a related rol

📌 Central Monitor (Bengaluru)
🏢 GSK
📍 Bengaluru

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