Clinical Trial Associate I

Allucent

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Role summary

Allucent, a contract research organization, seeks a Clinical Trial Associate I in Madrid to provide administrative support for clinical studies. The role involves managing electronic trial master files, investigator site files, and ensuring regulatory compliance across international clinical trials.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workable, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-03 (originally posted 2026-10-03). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

High school diploma or equivalent; bachelor's degree preferred
1+ year as CTA trainee or 2+ years in similar clinical research role
Knowledge of Good Clinical Practices and medical terminology
Fluency in Spanish and English, spoken and written
Proficiency in Microsoft Office and computer literacy
Ability to manage multiple projects independently with minimal oversight

What you'll be doing

Perform quality checks on documents before electronic trial master file submission
Prepare, maintain, and distribute investigator and pharmacy site files for site visits
Update and maintain site-level clinical trial management systems and generate reports
Prepare and track distribution of clinical trial supplies to investigational sites
Assist with feasibility activities and organization of investigator meetings as needed

Privacy & handoff

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