Experteer Overview
As Clinical Trial Associate I at Allucent, you support cross-site trial operations to ensure compliant, timely study execution. You’ll help manage essential trial documents and site files, contributing to inspection readiness and accurate data in TMF systems. Your work supports seamless collaboration with the CRA team and sponsors, enabling efficient regulatory adherence. This role offers hands-on experience in eTMF and site-level documentation within a general clinical trials environment.

Compensaciones / Beneficios
• Perform quality checks on documents for eTMF submissions to ensure completeness and accuracy
• Submit country/site level documents to eTMF Document Inbox and resolve rejections
• Assist with resolution of periodic QC findings for country/site eTMF
• Communicate with TMF Lead/Project Specialist on eTMF status




• Update Expected Documents List (EDL) in eTMF for country/site
• Maintain ISFs/eISFs, PSFs/ePSFs, and other files needed for Site Initiation Visits (SIVs)
• Prepare and maintain QC/Inventory Checklists for ISFs/PSFs to support CRA readiness for site visits
• Assist CRA with ISF/PSF vs. TMF reconciliation and support TMF inspection readiness
• Accurately updates site-level CTMS and assist with CTMS reports
• Prepare and distribute clinical trial supplies and track them
• Potential participation in feasibility/site identification activities
• Provide local support for Investigator Meetings or other study events

Responsabilidades
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Requisitos principales
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📌 Clinical Trial Associate I (Madrid)
🏢 Allucent
📍 Madrid