Clinical Research Associate (Belgium, Netherlands)

Allucent; Scherpenheuvel-Zichem; Sur place; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, pro-actively detect issues, and ensure studies are conducted per protocol, SOPs, and GCP/ICH guidelines.

You will lead monitoring activities, manage site relationships, and support startup activities, including contracting. Travel is required across Belgium and the Netherlands as needed.

Qualifications

• Independently monitor investigational sites, pro-actively detect issues, provide solutions to ensure studies comply with protocol, SOPs and GCP/ICH.
• Drive site activation, contracting, and startup activities for compliant study execution.
• Collaborate with sponsor and site teams across regulatory affairs and trials.

Responsabilités

• Independently manage monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.

Description du poste

At Allucent™ our mission is to shine a light on new therapies that improve lives. When you join our team, you'll use your unique skills, expertise, and knowledge to forge meaningful partnerships with clients while helping them turn groundbreaking ideas into life-changing treatments.

If you're passionate about advancing pharmaceuticals and biologics, fueled by an entrepreneurial spirit, and eager to collaborate with top minds across science, business, and operations, we'd love to connect. Together we can accelerate innovation and grow side by side, making a last impact on patients worldwide.

Together we SHINE. Find more information about our values.

The role

Bring your monitoring expertise to the forefront of innovation. We are looking for a Clinical Research Associate (CRA) to join our A-team. As a CRA at Allucent™, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.

As a CRA, you will take the lead on monitoring activities, owning your sites and relationships with investigators. You'll be the bridge between sponsor and site, ensuring trial integrity while being supported by a collaborative, experienced team. This includes work related to regulatory affairs, site activation processes—including contracting and start-up activities—to ensure smooth and compliant study execution. You will travel throughout Netherlands and/or Belgium.

Main responsibilities

• Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
• Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.