Remote Start-Up Associate II

Allucent seeks a Start-Up Associate II in Italy to coordinate local site start-up activities and manage regulatory submissions with RA/IEC/IRB, acting as the main point of contact for investigators and sites through early study phases.You will file documents in eTMF, prepare country-specific CTAs and budgets, negotiate with sites, and support the Global...

Allucent seeks a Start-Up Associate II in Italy to coordinate local site start-up activities and manage regulatory submissions with RA/IEC/IRB, acting as the main point of contact for investigators and sites through early study phases.You will file documents in eTMF, prepare country-specific CTAs and budgets, negotiate with sites, and support the Global...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*/remote) in Italy! The SUA coordinates and performs local site...

Allucent is seeking an experienced Regulatory Affairs Coordinator to support site start-up activities for clinical trials. You will manage regulatory documents, track milestones in CTMS/eTMF, and prepare local submissions to regulators in coordination with the Global Regulatory team.A Life Science degree and 2+ years in regulatory affairs are required, with...

Syneos Health, Inc. is hiring a Contract Management Assistant to support Site Start-Up activities, focusing on investigator site contracts, ethics submissions, and essential documents required for site initiation.You will collaborate with global Clinical Operations teams under the SSU Country Manager to ensure regulatory and contractual compliance. The role...

CTI Clinical Trial and Consulting Services in Italy seeks a Clinical Research Associate to serve as main CTI contact for assigned study sites and to conduct monitoring visits in line with ICH-GCP. You will support start-up activities, manage essential regulatory documents, participate in team meetings, and help ensure accurate IP storage and trial...

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyze clinical trials, ensuring data integrity and patient safety across sponsor-driven studies. You will monitor sites, review data, and contribute to study documentation, working with investigators and staff to maintain high-quality trial conduct.Ideal candidates have a...