Central Monitor
Company: GSK (GlaxoSmithKline)
Job Overview
You will join GSK’s Central Monitoring team to support Risk Based Quality Management across global clinical studies. The role focuses on centralized data review, analytics-driven risk identification, and collaboration with study teams to protect patient safety and ensure high-quality clinical data.
Key Responsibilities
- Perform centralized monitoring from study start to database lock
- Identify trends, risks, and data quality issues using analytics tools
- Communicate findings and corrective actions to study teams
- Maintain documentation and inspection readiness
- Support setup and maintenance of data analytics tools
- Train teams on Risk Based Monitoring and Quality Management
Basic Qualifications
- Bachelor’s degree in Life Science, Health, Statistics, or related field
- Minimum 3 years experience in clinical trials or clinical operations
- Experience in clinical data review or centralized monitoring
- Strong knowledge of ICH-GCP guidelines
- Excellent written and verbal English communication
Preferred Qualifications
- Experience with Risk Based Monitoring / RBQM
- Hands-on knowledge of tools like Spotfire, CluePoints, etc.
- Basic data skills (SQL, R, Python) or statistical interpretation
- Experience working across countries and time zones
What GSK Offers
- Hybrid working model (2–3 days office)
- Career growth in a global biopharma company
- Competitive salary & performance bonus
- Medical insurance, retirement benefits & paid leaves
- Supportive and inclusive work environment
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