Clinical Research Associate
Company: Randstad Belgium Agency
- Location: Flemish Region, Belgium
- Seniority: Mid level
- Employment type: Full-time
- Posted: 2 days ago
- Offer language: English
Job description
Contract Duration: Long-term project through December 2027
Location / Coverage: Diegem & Benelux
Mobility: High travel requirement (up to 80% on-site monitoring across the Benelux region)
Sector: Global Healthcare / Pharmaceutical & MedTech Leader
The Role
On behalf of a world-renowned pharmaceutical and healthcare company, we are seeking an experienced Clinical Research Associate (SCRA) to drive clinical site performance and data integrity across innovative medical device and combination product studies.
In this field-intensive position, you will be the primary operational liaison between internal study teams and investigational sites throughout the Benelux area, dedicating approximately 95% of your focus to hands-on site management and monitoring.
Key Responsibilities
- On-Site Oversight : conduct comprehensive site visits (selection, initiation, routine monitoring, close-out) ensuring full adherence to protocol, ICH-GCP, ISO/MDR guidelines, and local regulations.
- Subject Safety & Data Quality : safeguard patient well-being while verifying the accuracy, completeness, and integrity of clinical data.
- Site Collaboration & Problem-Solving : act as a trusted partner to Principal Investigators and site coordinators, proactively resolving issues and driving corrective actions (CAPA).
- Compliance & Trial Readiness : ensure Investigator Site Files (ISF) and regulatory documentation remain inspection-ready. Support enrollment and patient retention initiatives.
Requirements
- Experience : minimum 4+ years of recent, independent on-site monitoring experience as a CRA/SCRA.
- Device Expertise : demonstrated monitoring experience with Medical Devices or combination products is strictly required.
- Mobility : willingness and readiness to travel up to 80% of the time across investigational sites in Belgium, the Netherlands, and Luxembourg.
- Languages : fluent in English & good working knowledge of Dutch
- Education: Bachelor’s degree in Life Sciences, Nursing, or a related biological discipline.
- Competencies: Strong organizational skills, autonomy in managing multi-site timelines, solid understanding of clinical systems (CTMS, eCRF, eTMF), and impactful communication skills.
Apply Now
Interested in driving high-standard clinical studies across the Benelux within an industry-leading environment? Submit your updated CV in English to discuss the opportunity.
