Clinical Trial Associate (entry level)

☞ PharmiWeb.Jobs

Ver: 135

Día de actualización: 17-11-2025

Ubicación: Brussels Brussels Capital

Categoría: R & D IT - Software

Industria: Staffing Recruiting

Posición: Entry level

Tipo de empleo: Full-time

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Contenido de trabajo

PermanentFull timeHybrid (Brussel region)RoleThe tasks For this hybrid role, the tasks will include but are not limited toThe CTA will be delivering support to the Early-Stage Development Europe Operational team. He/she will be providing operational support and project support. This will include responsibility for in-house activities as well as for compliance with processes required to initiate, maintain, support, and close out the early-stage clinical trials managed by the department. He/she will also carry out tasks for the support of clinical grants. The company The company is a Clinical Research Organization specialized in clinical project management with a great values and corporate culture.Assemble and provide support for timely Clinical Trial Submissions and availability of Essential Documents for clinical trials. Create Essential Documents Repository. Assemble and track availability of all essential documentation required for study conduct. Provide professional presentation of study materials for investigator/vendor or country operations meetings Liaise with sites and in house departments to ensure appropriate regulatory follow-up Organization and documentation (minutes) of project team meetings where need be Operational and project support activities, including, but not limited to: Update, maintain and monitor CTMS to allow accurate project management, regulatory reporting and clinical grants payments Follow-up/check final accountability of IMP and return or destruction as appropriate Possibility for SME roles: CTMS, TMF steward, SIP, CLMS, Safety reporting tracking Review study budgets/clinical trial agreements for consistency with study protocol Updating of clinical and study planning databases Review study budgets/clinical trial agreements for consistency with study protocol Clinical trial payments and payment tracking Compliance checks Maintenance of trackers Your profileBachelor degree (e.g. medical assistant, or paramedical education) or relevant work experience in clinical research field Advanced computer skills: e.g. professional using of MS Office programs for daily business including Excel Advanced communication skills (written and verbal) in local languages and English Understanding and knowledge of study protocols and study working documents, lab manuals, etc An understanding of the clinical research processes Preferably, an understanding of the ICH/GCP (international good clinical practice guidelines and harmonization) and local clinical trial regulations To explore this job opportunity further, please apply now or contact Wentworth Life Sciences to learn more about this exciting career move.
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Plazo: 01-01-2026

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