Central Monitor US/UK/BE/PL

JR United Kingdom; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

Join a leading life sciences recruiter as a Central Monitor, driving advancements in clinical trials and enhancing patient safety. Utilize data and technology to optimize monitoring strategies and ensure clinical studies reach their full potential. Collaborate with study teams and mentor data analysts to improve operational efficiency.

Qualifications

• Solid understanding of clinical trial phases and regulatory guidance.
• Strong experience in clinical operations, RBQM, or Central Monitoring.

Responsibilities

• Guide study teams in identifying critical data and conducting Risk Assessments.
• Determine Key Risk Indicators and enhance study success.
• Investigate atypical data patterns and communicate findings.

Skills

Data Analytics

Critical Thinking

Education

Bachelor's degree in a scientific or business-related discipline

Job description

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 the 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:

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

Key Skills and Requirements:

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

If you are having difficulty applying or have questions, please contact Heidi Hennigan at [emailprotected].

Apply Now:

If you're interested in this exciting opportunity, please click 'Apply' or request a callback at the top of this page to speak with one of our specialists.

Proclinical is a leading life sciences recruiter focused on connecting exceptional people with top positions worldwide. We act as an Employment Agency for this vacancy.

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