We are looking for a CTA with experience based in Madrid to support on the management and maintenance of documentaion related with the protocols and studies assigned. Working fully outsourced to one of our global pharmaceutical clients, the Clinical Trial Assistant plays a fundamental role in the successful execution of global clinical trials. Operating within the scope of the Clinical Development Plan, ICH-GCP guidelines and in accordance with the study protocol, local and international regulatory requirements and company procedures, the Clinical Trial Assistant (CTA) works to support the completion and coordination of various logistical and administrative tasks. The Clinical Trial Assistant's (CTA) work is varied, fast-paced and quality focused. Maintaining constructive relationships with site staff (eg Investigators, Study Coordinators etc) as well as with colleagues within the organisation, the Clinical Trial Assistant is responsible for the maintenance and updating of the Trial Master File (and preparation for relevant QC checks when applicable) also falls within the CTA's remit. Functioning as a key component of the clinical study team, the Clinical Trials Assistant (CTA) may also be responsible for scheduling meetings, updating Excel trackers, coordinating the translation of site documents and providing ad-hoc support as appropriate.