Clinical Research Associate
External
Merck · - North Brabant, NetherlandsPrepare for this interview
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About the role
As a Clinical Research Associate, you will independently manage and monitor clinical study activities at site level. You will ensure that clinical studies are conducted in compliance with study protocols, Good Clinical Practice (GCP), VICH guidelines and applicable regulatory requirements. You will collaborate closely with the Clinical Study Team, Data Management and external partners to ensure accurate data collection, proper documentation and timely execution of study activities. Tasks and responsibilities include but are not limited to Conduct site visits (initiation, interim, and close-out) across CROs, veterinary clinics and farms, ensuring study compliance. Prepare, maintain and review study documentation, including study files and CRFs, in collaboration with the study team. Support site selection and assist in engaging investigators, laboratories and external partners. Train site personnel on study protocols, GCP and procedural requirements. Manage study materials and sample logistics, including shipment, tracking and inventory control. Ensure accurate and complete documentation of study activities, including deviations, adverse events and site communications. Review and verify study data for accuracy and completeness, including EDC entry, query resolution and data validation. Oversee proper handling, storage, and accountability of investigational products. Contribute to quality and operational excellence by supporting vendor management, conducting quality checks, assisting with issue resolution and mentoring junior team members. Your profile Bachelor's degree in a relevant biological or life sciences field. Proven experience in a clinical research role, preferably in animal health or related field. Strong understanding of Good Clinical Practice (GCP) and clinical study processes. Experience with Electronic Data Capture (EDC) systems preferred. Proficiency in Microsoft Office applications. Excellent command of Dutch and English, both written and spoken. Strong organizational skills with attention to detail and quality. Ability to work independently and collaboratively in a cross-functional environment. Willingness and ability to travel up to 50% to study sites.
Benefits
Additional Information
Job Description Step into a forward-thinking Clinical Research team at the forefront of innovation in animal health, delivering impactful studies across Europe. Join us in Boxmeer as a: Clinical Research Associate Welcome in our team Our Clinical Research team is responsible for the execution and monitoring of clinical field studies across Europe that support the development of animal health products. We work closely with internal and external stakeholders including Contract Research Organizations (CROs), veterinary clinics, farms, and laboratories to ensure high-quality data and compliance with regulatory standards. The team is part of the global Research & Development organization, contributing to innovative solutions for animal health.
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