Clinical Research Associate (Belgium, Netherlands)
Quick Summary
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,
You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative envi
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.
Responsibilities
~1 min read- →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.
- →Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
- →Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
- →Activities around regulatory affairs, site activation and study-startup.
You’re an experienced CRA ready to take the next step with a company that truly values your expertise and independence. You thrive in an agile, collaborative environment and want to be part of a team making a real impact.
- Experience in leading monitoring activities in complex trials with a minimum of 2 years’ experience.
- Strong understanding of ICH-GCP and regulatory guidelines.
- Clear and confident communicator in English and Dutch.
- Comfortable working independently and managing priorities.
- Willingness to travel, as required (8 DOS per month).
What We Offer
~1 min read*Our in-office work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices.
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
#LI-BL1
Location & Eligibility
Listing Details
- Posted
- July 21, 2026
- First seen
- August 12, 2026
- Last seen
- August 12, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 22%
- Scored at
- August 12, 2026
Signal breakdown

Allucent is a global clinical research organization (CRO) dedicated to helping small and mid-sized biotech companies bring new therapies to light by providing comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology.
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