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For Companies At a Glance
- Tasks: Transform clinical research by optimising monitoring strategies and ensuring studies run smoothly.
- Company: CluePoints is revolutionising clinical trials with a focus on patient safety and data quality.
- Benefits: Enjoy flexible work, team events, training opportunities, and a competitive salary.
- Why this job: Make a real impact in clinical trials while working in a dynamic, award-winning tech environment.
- Qualifications: 3+ years in clinical trials, strong data analytics skills, and a relevant degree.
- Other info: Join a diverse, international team and help shape the future of clinical trial monitoring.
The predicted salary is between 28800 - 48000 £ per year.
Overview
Join to apply for the 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. 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
What We’re Looking For:
- Experience: 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).
- Knowledge: 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.
- Skills: Data analytics aptitude and critical thinking skills to identify risks and drive decisions based on data.
- Education: Bachelor’s degree or higher in a scientific or business-related discipline (or equivalent experience).
Job Responsibilities
- Enable Successful Platform Implementation: 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) that enhance study success.
- Provide Expert Coaching & Guidance: Coach customers on implementing our platform and product methodologies, helping them optimize monitoring resources to address study-specific risks. Mentor data analysts to define KRIs based on risk assessments, protocols, and study documentation.
- Signal Management & Communication: 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.
- Drive Continuous Improvement: Document and share lessons learned to foster cross-study knowledge sharing. Collaborate with the Product team to test and validate system updates, ensuring that new features meet the needs of our customers.
Job Benefits
- Flexibility is part of our DNA
- Many activities are organized during the year such as team lunches, happy hours, team buildings, holiday parties and celebrations
- Learning and development: access to online training materials, certifications sponsored by the company, personal growth plans, and career paths
- International, English-speaking working environment with a diverse team
- Challenging and rewarding work in a fast-paced technology scale-up with awards
- Competitive salary and benefits
Additional Details
- Seniority level: Entry level
- Employment type: Full-time
- Job function: Consulting
- Industries: Pharmaceutical Manufacturing and Software Development
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Central Monitor (US-BE-PL-UK) employer: CluePoints
Contact Detail:
CluePoints Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Central Monitor (US-BE-PL-UK)
✨Tip Number 1
Familiarise yourself with the latest trends in Risk-Based Quality Management (RBQM) and clinical trial monitoring. Understanding how these concepts are evolving will help you speak confidently about your insights during interviews.
✨Tip Number 2
Network with professionals in the clinical trials field, especially those who have experience in central monitoring. Attend industry conferences or webinars to make connections that could lead to referrals or insider information about the role.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences where you successfully identified risks and implemented solutions in clinical trials. This will demonstrate your practical knowledge and problem-solving skills to potential employers.
✨Tip Number 4
Stay updated on regulatory guidelines such as ICH GCP. Being well-versed in these regulations will not only enhance your credibility but also show your commitment to maintaining high standards in clinical research.
We think you need these skills to ace Central Monitor (US-BE-PL-UK)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trials, particularly focusing on your understanding of study phases and regulatory guidance. Use specific examples to demonstrate your skills in data management and risk assessment.
Craft a Compelling Cover Letter: In your cover letter, express your passion for clinical research and how your background aligns with the role of Central Monitor. Mention your experience with Risk-Based Quality Management and how you can contribute to CluePoints' mission.
Showcase Data Analytics Skills: Emphasise your data analytics aptitude in both your CV and cover letter. Provide examples of how you've used data to identify risks and drive decisions in previous roles, as this is crucial for the position.
Highlight Continuous Improvement Initiatives: Discuss any experiences where you've contributed to continuous improvement in clinical operations. This could include documenting lessons learned or collaborating with teams to enhance processes, which aligns with the responsibilities of the role.
How to prepare for a job interview at CluePoints
✨Understand the Role
Make sure you have a solid grasp of what a Central Monitor does. Familiarise yourself with clinical trial phases, risk-based quality management, and the specific responsibilities outlined in the job description. This will help you articulate how your experience aligns with their needs.
✨Showcase Your Data Skills
Since the role heavily involves data analytics, be prepared to discuss your experience with data management and medical data review. Bring examples of how you've used data to identify risks and drive decisions in past projects.
✨Prepare for Scenario Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past experiences where you had to address atypical data patterns or conduct risk assessments, and be ready to explain your thought process and outcomes.
✨Demonstrate Your Passion
CluePoints is looking for someone who is passionate about improving clinical trials. Share your motivation for wanting to work in this field and how you see yourself contributing to patient safety and data quality through your role as a Central Monitor.
