We’re seeking a Senior Central Monitor to join our team! In this role, you’ll play a key part in ensuring the quality and integrity of clinical trial data through centralised monitoring activities, statistical data review, and proactive risk management.
🧠 Key Responsibilities:
Lead the development of Risk-Based Quality Management (RBQM) plans
Conduct study risk assessments and identify potential issues
Perform centralised statistical monitoring and data analysis
Facilitate monthly RBQM meetings and document findings
Ensure data quality and integrity through proactive monitoring
Collaborate with cross-functional teams to support study deliverables
Prepare detailed reports and presentations on monitoring activities
🔍 Key Responsibilities
Lead the development and implementation of RBQM plans
Conduct study risk assessments and proactively identify issues
Perform centralised statistical monitoring and data analysis
Facilitate monthly RBQM meetings and document key findings
Ensure data quality and integrity across clinical studies
Collaborate with cross-functional teams to support study deliverables
Prepare reports and presentations summarising monitoring activities
Mentor and guide junior team members in best practices
🎓 Qualifications & Requirements
Education:
Bachelor’s degree in Life Sciences, Statistics, Clinical Operations, or a related field
Experience:
Minimum 5 years of experience in clinical monitoring or related roles
Solid understanding of ICH GCP guidelines and the clinical development process
Skills:
Expertise in RBQM principles and methodologies
Proficiency in statistical analysis and data monitoring tools
Strong analytical, communication, and organisational skills
Experience mentoring or training junior staff
Preferred:
Prior experience in a CRO as a Central Monitor
Excellent written and verbal English skills
📊 What You’ll Do
Lead and implement RBQM plans
Conduct risk assessments and identify process improvements
Perform centralised data and statistical reviews
Drive data integrity initiatives and ensure regulatory compliance
Prepare comprehensive study reports and share actionable insights
🌟 Why Join Us?
Work on complex, high-impact clinical trials
Be part of a collaborative, global research environment
Opportunity to lead and mentor within a growing team
Exposure to cutting-edge RBQM and data-driven monitoring methods
📍 Location
Flexible / Hybrid options available (based on company policy)
Industry: Clinical Research & Data Management
Job Type: Full-time
📧 How to Apply
Ready to take the lead in central monitoring?
👉 Apply here: LinkedIn Job Link