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Clinical Trial Assistant - Madrid - Crovelis
Descripción
Clinical Trial Assistant (CTA)¿Interesado en saber más sobre este trabajo?
Desplácese hacia abajo y descubra qué habilidades, experiencia y cualificaciones académicas se necesitan.
Experience:
Minimum 2 years managing TMF in clinical trials
CROVELIS is building a globally focused internal CRO to deliver exceptional clinical trial results. We are a high-growth, fast-paced, and agile organization that values teamwork, collaboration, and proactive problem-solving.
At CROVELIS, diversity, creativity, and professional development are core pillars, and we foster a supportive, inclusive environment for all employees.
Assist in the collection, review, and tracking of essential documents for clinical trials to ensure timely and compliant study startup and maintenance.
Conduct periodic quality checks of TMF contents to ensure all documentation is audit-ready and compliant with regulatory guidelines.Manage and process invoices related to clinical trials, ensuring accuracy and timely submission to vendors.
Assist in tracking budgets, expenditures, and financial milestones across different clinical studies, ensuring their accurate documentation within the SAP system.
Liaise with vendors and service providers to assist in qualification processes and address any discrepancies in billing or financial agreements.
Manage financial and billing processes efficiently within clinical trials.Bachelor's degree in Life Sciences, related field, or equivalent experience.
At least 2 years of hands-on experience managing TMF in clinical trials.
Experience in billing or financial management within a clinical trials setting.
Familiarity with SAP system.
Familiarity with ICH-GCP guidelines and clinical trial documentation processes. xugodme
Strong proficiency in financial systems and MS Office Suite (Word, Excel).
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Clinical Trial Assistant
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