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Leyden Labs

Senior Clinical Trial Associate

Leyden Labs

Freelance Sr. Clinical Trial Associate assisting Clinical Trial Teams in the Netherlands with project tracking and document management.

Posted 6/24/2026contractRemote • 🇳🇱 NetherlandsSeniorWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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

Requirements

What you’ll need
  • 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

Comp & perks
  • Occasional travel to the Leiden office could be requested 1-2 times per month.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical trial administrationproject trackingdocument managementGood Clinical Practices (GCP)International Conference on Harmonization (ICH) GuidelineseTMFEDCIRT/RTSMCTMS systemsMicrosoft Office
Soft Skills
communication skillsteam supportindependent managementorganizational skillsattention to detail