Clinical Trials Monitoring Specialist

IQVIA is seeking a CRA to monitor and manage clinical research sites in Italy, ensuring compliance with study protocols and regulations. The ideal candidate will hold a Master's degree in Life Sciences and have CRA certification. Responsibilities include conducting site monitoring visits, ensuring data integrity, and managing study documentation....

Join Our Team and Shape the Future of Clinical Research! At Fortrea , we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist, you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our...

Fortrea in Turbigo, Italy is looking for a Site Budget & Contract Specialist to streamline clinical trials and ensure compliance with global regulations. In this role, you will negotiate site agreements and manage budgets to support innovative clinical research efforts.The ideal candidate should have 2–4 years of relevant experience and a Bachelor's...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and...

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. Responsibilities Leads the project team, ensuring the project is delivered according to planned scope and timelines in accordance with the...

TRIO - Translational Research in Oncology is looking for an experienced Senior CRA to join their passionate team in Italy. This full-time, home-based role requires expertise in oncology research and monitoring experience in clinical trials. You will conduct site visits, ensure adherence to GCP guidelines, and mentor junior CRAs. The position offers a...

Translational Oncology Research, LLC is seeking an experienced Senior Clinical Research Associate to join their Monitoring Resources team. This full-time position is home-based in Italy and involves conducting site visits, ensuring regulatory compliance, and mentoring junior team members.The successful candidate will have at least 5 years of CRA experience,...

At AllucentTM, 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. Responsibilities * Leads the project team, ensuring the project is delivered according to planned scope and timelines in accordance with the...

Fortrea in Turbigo, Italy is looking for a Site Budget & Contract Specialist to streamline clinical trials and ensure compliance with global regulations. In this role, you will negotiate site agreements and manage budgets to support innovative clinical research efforts. The ideal candidate should have 2–4 years of relevant experience and a...