Central Monitor US/UK/BE/PL

TN United Kingdom; London; On-site; GBP 40,000 - 80,000; Full time

Job summary

Join a forward-thinking company as a Central Monitor, where you'll play a pivotal role in advancing clinical trials and enhancing patient safety. This exciting position allows you to leverage data and innovative technology to optimize monitoring strategies and elevate study performance. If you're passionate about making a meaningful impact in clinical research and thrive in a dynamic environment, this opportunity is perfect for you. Be part of a team that values innovation and collaboration, and help shape the future of clinical studies across multiple regions.

Qualifications

• Solid understanding of clinical trial phases and design.
• Experience in clinical operations and RBQM.

Responsibilities

• Guide study teams in identifying critical data and conducting risk assessments.
• Mentor data analysts in defining Key Risk Indicators (KRIs).
• Investigate atypical data patterns to improve operational efficiency.

Skills

Clinical trial phases

Clinical operations

Risk-Based Quality Management (RBQM)

Data analytics

Critical thinking

Education

Bachelor's degree in a scientific discipline

Bachelor's degree in a business-related discipline

Job description

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Join our client's team as a Central Monitor and become a key driver in advancing clinical trials and enhancing patient safety. In this role, you'll harness the power of data and cutting-edge technology to optimize monitoring strategies and elevate study performance. If you're driven by innovation and committed to making a meaningful difference in clinical research, we'd love to have you on our team.

Proclinical is seeking a Central Monitor to join our client's team and make a significant impact on clinical trials and patient safety across US, UK, Belgium, and Poland. In this role, you will utilize data to optimize monitoring strategies and ensure clinical studies reach their full potential.

Responsibilities:

• Guide study teams and data analysts in identifying critical data and conducting Risk Assessments.
• Determine Key Risk Indicators (KRIs) and Quality Tolerability Limits (QTLs) to enhance study success. Coach customers on implementing platform methodologies and optimizing monitoring resources.
• Mentor data analysts in defining KRIs based on risk assessments and study documentation.
• Assess and address risks, providing actionable insights to customer study teams.
• Investigate atypical data patterns and communicate findings to improve operational efficiency.
• Document and share lessons learned for cross-study knowledge sharing.
• Collaborate with the Product team to test and validate system updates.

Key Skills and Requirements:

• Solid understanding of clinical trial phases, design, execution, and regulatory guidance.
• Strong experience in clinical operations, RBQM, or Central Monitoring.
• Aptitude for data analytics and critical thinking skills.
• Bachelor's degree or higher in a scientific or business-related discipline or equivalent experience.