Allucent is a general full-service contract research organization dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light.

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Our clients have new therapeutic ideas but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in patients’ lives.

We are looking for a Clinical Trial Associate I to join our team in Madrid - Spain The Clinical Trial Associate (CTA)



acts as the primary administrative support to Allucent clinical study teams at Country/Site level, to support Clinical Trial Operations and Sponsors, thus ensuring that the clinical trial is conducted in accordance with international regulatory and local regulatory and ethical laws, and guidelines for Good Clinical Practice and Standard Operating Procedures. The CTA also assists the study team with the day-to-day conduct of international clinical studies.

Location: Madrid, Spain

Workplace: Office based

Key Responsibilities

eTMF
- Performs quality check of documents prior to eTMF submission to ensure the documents meet specifications to be complete and accurate for filing.
- After quality check acts as Document Submitter and submits country and site level documents to eTMF Document Inbox. Resolves rejections.
- Assists with resolution of periodic QC findings for country and site eTMF.
- Communicates with the TMF Lead / Project Specialist to follow-up on c

📌 Clinical Trial Associate I (Madrid)
🏢 Allucent
📍 Madrid