Clinical Trial Start-Up Lead: Site Activation Expert

ICON Clinical Research in Italy seeks a professional to lead day-to-day site start-up and activation activities, ensuring quality outcomes and regulatory compliance. You will drive site activation plans, sponsor communications, and milestone tracking, while managing priorities across projects.The role requires a life sciences bachelor's degree, 4+ years in...

Your impact begins here As Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps...

Overview In this role you support the local study team in Italy from start-up to close-out, ensuring trial documentation, progress tracking, vendor coordination, and timely investigator payments. You contribute to compliance and inspection readiness so new treatments reach patients with serious chronic diseases. You’ll work within the Clinical Development...

As Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps trials compliant and...

As Clinical Trial Administrator, you will keep clinical trials in Italy moving with accuracy and pace. Based in Rome, you will support the local study team from start-up to close-out – managing trial documentation, tracking progress, coordinating vendors and making sure investigator sites’ payments are on time. Your work keeps trials compliant and...

OverviewAs an RSU Specialist, you will lead country-specific site activation and regulatory activities within IQVIA's FSP team in Italy. You will act as the primary liaison for investigative sites and project teams, ensuring compliant, timely site activation and regulatory documentation. You will leverage local regulatory expertise to support timelines, risk...

Thermo Fisher Scientific (PPD) is seeking a Senior Clinical Team Manager to lead start-up and clinical deliverables for oncology and related therapy areas. You will coordinate a regional or country team, ensuring training, tracking and quality systems for the clinical management team. As Sr.CTM you own start-up deliverables, anticipate problems, and drive...

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...

Overview In this role you support regional clinical study delivery to ensure trials run on time, within budget, and to quality standards. You collaborate with the Regional Clinical Study Manager, global teams, and site staff to coordinate feasibility, start-up, TMF, and site communications. You gain hands-on experience in clinical operations and regulatory...