SolCur

www.solcur.com

1 Job

19 Employees

About the Company

Connecting talent and companies in clinical research with purpose. At SolCur, we go beyond the resume. We believe in the power of genuine human connections, paired with professionalism and sustainability. Our mission? To help companies find top talent and guide professionals toward their next career opportunity. Backed by expertise and a strong network, we create matches that don’t just work—they last. Because at SolCur, the right fit is the foundation for long-term success.

Listed Jobs

Company Name: SolCur
Job Title: Clinical Trial Assistant
Job Description: **Job Title:** Clinical Trial Assistant **Role Summary:** Provide comprehensive administrative and operational support to the Clinical Research Team (CRAs, CPMs, Medical Department) to ensure smooth execution of clinical trials, maintain documentation compliance, and facilitate effective communication with internal and external stakeholders. **Expectations:** - Deliver accurate, timely documentation and filings. - Communicate professionally in English and an additional language (Dutch or French). - Maintain organized records in CTMS and related systems. - Support logistics, travel, and meeting coordination. - Demonstrate strong attention to detail and teamwork. **Key Responsibilities:** - Perform general administrative tasks for the clinical research team. - Prepare, update, and electronically file trial documents; assemble study binders. - Assist in preparing and submitting packages to Ethics Committees/IRBs. - Manage correspondence with internal and external parties (English). - Attend meetings, record minutes, and draft reports. - Coordinate investigator and team meetings, including travel arrangements. - Enter, update, and track data in the Clinical Trial Management System (CTMS). - Handle study supplies: shipping, tracking, inventory control. **Required Skills:** - Proficiency in English and Dutch or French (written and spoken). - Experience with CTMS, IRT/IXRS, eTMF, and other trial‑progress systems. - Strong knowledge of ICH‑GCP and EU Clinical Trial Directives. - Advanced Microsoft Office skills (Word, Excel, PowerPoint, Outlook). - Excellent organizational, multitasking, and detail‑orientation abilities. - Ability to work collaboratively in a team environment. **Required Education & Certifications:** - Bachelor’s or Master’s degree in a relevant field (or equivalent experience). - 1–3 years of experience in clinical or medical administration. - Familiarity with GCP guidelines and clinical trial regulations (formal certification not mandatory but preferred).