Clinical Trial Start-Up Lead: Site Activation Expert

What You Will Do: You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes. Key responsibilities include: Lead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution. Oversee day-to-day delivery of all aspects...

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...

Overview As 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,...

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...

## Regulatory and Start Up Specialist - ItalyApply: Milan, Italy: Full time: Posted Today: R1572752### RSU Specialist**Level:** Senior Associate **Location:** Italy (Home Based) ### About IQVIAIQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights to the life sciences industry. With more...

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...

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.In this role your key tasks will include:Track relevant information, data, progress and milestones in CTMS and/or other tracking tools covering...

Based in Rome, Novo Nordisk A/S is seeking a Clinical Trial Administrator to keep Italy's trials moving with accuracy and pace. You will support the local study team from start-up to close-out, managing trial documentation, tracking progress, coordinating vendors and ensuring timely investigator site payments. You will work within the Business Operations...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...