Description:

Join Excelya, a dynamic company in translational research.
Role focuses on ensuring quality, compliance, and inspection readiness of the electronic Trial Master File (eTMF) across global clinical trials.

Requirements:

Bachelor’s or Master’s degree in Health Sciences, Life Sciences, or related field.
Strong experience in clinical trial documentation management.
Hands-on experience with Veeva Vault TMF (mandatory).
Strong understanding of the DIA TMF Reference Model.
Experience with TMF metrics, KPIs, and dashboards.
Knowledge of ICH/GCP guidelines and regulatory requirements.
Fluent in English (written and spoken).

Work in a young, ambitious health company aiming to be Europe’s leading mid-size CRO.
Opportunity to evolve through diverse projects and collaborate with experts in the field.