CluePoints
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Central Monitor (US-BE-PL-UK)
role at
CluePoints .
Are you ready to make a real impact on the future of clinical trials and patient safety? As a Central Monitor, you will play a pivotal role in transforming clinical research through our industry-leading platform and product suite. If you’re passionate about leveraging data, optimizing monitoring strategies, and ensuring clinical studies run at their highest potential, we want you to be part of our team!
About Us At CluePoints, we’re pioneers in Risk-Based Quality Management (RBQM), and our solutions are revolutionizing the way clinical trials are managed. With a strong commitment to patient safety, data quality, and operational excellence, we empower study teams and customers to achieve their goals faster, smarter, and more efficiently.
Job Description As a Central Monitor, you’ll be a key player in shaping the future of clinical trial monitoring and ensuring our solutions deliver maximum value to our customers.
Job Requirements
Minimum of 3 years’ experience working in clinical trials with a solid understanding of study phases, design, execution, and regulatory guidance (e.g., ICH GCP).
Strong experience in clinical operations, RBQM or Central Monitoring, including data management and medical data review. Familiarity with clinical trials across multiple therapeutic areas is a plus.
Data analytics aptitude and critical thinking skills to identify risks and drive decisions based on data.
Bachelor’s degree or higher in a scientific or business-related discipline (or equivalent experience).
Job Responsibilities
Guide study teams and data analysts in identifying critical data, conducting comprehensive Risk Assessments, and determining Key Risk Indicators (KRIs) and Quality Tolerability Limits (QTLs).
Coach customers on implementing our platform and products methodologies, helping them optimize monitoring resources to address study-specific risks.
Assess and address risks, providing actionable insights to customer study teams, investigate atypical data patterns, define follow-up actions, and communicate findings to guide decision‑making and improve operational efficiency.
Document and share lessons learned to foster cross-study knowledge sharing; collaborate with the Product team to test and validate system updates, ensuring new features meet customer needs.
Job Benefits
Flexibility is part of our DNA.
Learning, training and personal growth: access to online training materials, certifications sponsored by the company, personal growth plans, and career paths.
Challenging and rewarding job in an ambitious fast‑paced technology scale‑up that has received many national and international awards.
Competitive salary & benefits such as Pension Plan, Health Insurance, Working from Home allowance, Cafeteria Plan, Legal Holidays, Bonus Plan.
Seniority level
Entry level
Employment type
Full‑time
Job function
Analyst and Consulting
Industries
Pharmaceutical Manufacturing and Software Development
Referrals increase your chances of interviewing at CluePoints by 2x.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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Central Monitor (US-BE-PL-UK)
role at
CluePoints .
Are you ready to make a real impact on the future of clinical trials and patient safety? As a Central Monitor, you will play a pivotal role in transforming clinical research through our industry-leading platform and product suite. If you’re passionate about leveraging data, optimizing monitoring strategies, and ensuring clinical studies run at their highest potential, we want you to be part of our team!
About Us At CluePoints, we’re pioneers in Risk-Based Quality Management (RBQM), and our solutions are revolutionizing the way clinical trials are managed. With a strong commitment to patient safety, data quality, and operational excellence, we empower study teams and customers to achieve their goals faster, smarter, and more efficiently.
Job Description As a Central Monitor, you’ll be a key player in shaping the future of clinical trial monitoring and ensuring our solutions deliver maximum value to our customers.
Job Requirements
Minimum of 3 years’ experience working in clinical trials with a solid understanding of study phases, design, execution, and regulatory guidance (e.g., ICH GCP).
Strong experience in clinical operations, RBQM or Central Monitoring, including data management and medical data review. Familiarity with clinical trials across multiple therapeutic areas is a plus.
Data analytics aptitude and critical thinking skills to identify risks and drive decisions based on data.
Bachelor’s degree or higher in a scientific or business-related discipline (or equivalent experience).
Job Responsibilities
Guide study teams and data analysts in identifying critical data, conducting comprehensive Risk Assessments, and determining Key Risk Indicators (KRIs) and Quality Tolerability Limits (QTLs).
Coach customers on implementing our platform and products methodologies, helping them optimize monitoring resources to address study-specific risks.
Assess and address risks, providing actionable insights to customer study teams, investigate atypical data patterns, define follow-up actions, and communicate findings to guide decision‑making and improve operational efficiency.
Document and share lessons learned to foster cross-study knowledge sharing; collaborate with the Product team to test and validate system updates, ensuring new features meet customer needs.
Job Benefits
Flexibility is part of our DNA.
Learning, training and personal growth: access to online training materials, certifications sponsored by the company, personal growth plans, and career paths.
Challenging and rewarding job in an ambitious fast‑paced technology scale‑up that has received many national and international awards.
Competitive salary & benefits such as Pension Plan, Health Insurance, Working from Home allowance, Cafeteria Plan, Legal Holidays, Bonus Plan.
Seniority level
Entry level
Employment type
Full‑time
Job function
Analyst and Consulting
Industries
Pharmaceutical Manufacturing and Software Development
Referrals increase your chances of interviewing at CluePoints by 2x.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr