Freeing humanity from the burden of respiratory viruses
Senior Clinical Trial Associate
Location
Netherlands
Posted
1 day ago
Salary
0
Seniority
Senior
Job Description
Senior Clinical Trial Associate
Leyden Labs
• Assist the Clinical Trial Teams in ensuring the most effective and efficient conduct of clinical trials by providing administrative and project tracking support • Support the preparation, handling, distribution, collection and archiving of clinical study documents and reports, including contracts and invoices • Ensure that all study files are periodically reviewed for completeness and maintained in accordance with Good Clinical Practices, applicable regulations and company procedures • Interface with internal colleagues and external vendors and partners • Work closely with the Clinical Operations Team to support the effective execution of clinical studies and maintain high standards of quality and compliance
Job Requirements
- Master's degree in a life science related field
- At least 5 years’ experience in a CTA role in a bio-pharmaceutical and/or CRO environment
- Proven training in/knowledge of GCP and International Conference on Harmonization (ICH) Guidelines
- Previous experience working with eTMF, EDC, IRT/RTSM, CTMS systems
- Ability to independently manage documentation and team support needs
- Computer skills including working knowledge of Microsoft Word, Excel, PowerPoint, and SharePoint
- Excellent verbal and written communication skills in English
- Currently residing in the Netherlands with EU work authorization
- Available for 32-40 hours per week until December 2026.
Benefits
- Occasional travel to the Leiden office could be requested 1-2 times per month.
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