Central Monitor, Cluepoints | VINDAZO in België

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Plaats

België
0000
België
België

Contract

Vooltijds, Onbepaalde duur

Datum gepubliceerd

2025-11-28

Online to:

2026-01-27
EUR 20.00 HOUR

Central Monitor

Cluepoints
België
9 uren geleden

Description
Company Description
At CluePoints, we're on a mission to revolutionize clinical trials through cutting-edge Risk-Based Quality Management (RBQM) and Data Quality Oversight solutions. Our award-winning platform helps pharmaceutical, and biotech companies bring safer, more effective treatments to patients faster.
We're proud to be an ambitious, fast-growing technology scale-up with a dynamic and diverse international team representing more than 20 nationalities. Collaboration, flexibility, and continuous learning are part of our DNA — at CluePoints, you'll find a culture where you can grow, make an impact, and have fun along the way
The Role
We're looking for a Central Monitor to join our Professional Services team and contribute to our mission of transforming clinical research through data-driven insights. 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
*This position is a hybrid role that requires 2-3 days in office.*
Requirements
What You'll Bring

Bachelor's degree or higher in a scientific or business-related discipline (or equivalent experience) with a 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.

Nice to Have

Experience in life sciences or technology scale-ups.
Familiarity with GCP or data analytics tools.
Additional language skills.

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