ppIn this role you lead the initiation of clinical trials, ensuring regulatory compliance and supporting the advancement of new treatments.
You collaborate across the Study Startup team, CROs, and Clinical Operations to optimize site activation timelines and maintain accurate documentation.
You will monitor site performance, address activation delays, and ensure eTMF quality.
This position offers the chance to impact trial timelines and improve SSU processes in a values-driven environment.
/pulliHealth and wellbeing programmes /liliRetirement and pension plans /liliLife assurance and disability coverage /liliEmployee assistance programmes /liliLearning and development opportunities /liliCoordinate site start-up and activation activities and deliverables /liliCollaborate with internal Study Startup team, CROs, Clinical Operations,



and TAU partners to improve SSU metrics /liliEnsure adherence to SSU standards across projects /liliIdentify and elevate potential site activation delays /liliTrack actions and communications to meet study/site timelines /liliResolve escalated issues in partnership with CROs and Clinical Operations /liliProvide feedback on site performance metrics to management /liliEnsure accuracy and completeness of the eTMF for assigned sites during start-up /liliBS degree or international equivalent /lili2+ years of experience in clinical research Site Start Up within pharma, CRO, or relevant vendor /liliAbility to translate data into informed decisions /liliKnowledge of clinical study protocols and essential documents /liliStrong organizational, decision-making, communication, and negotiation skills /liliProficiency in Microsoft Excel, Word, and PowerPoint /li /ul /p #J-*****-Ljbffr

📌 Study Start Up Associate Ii (Milano)
🏢 Experteer Italy
📍 Milano