Country Study Start-Up Specialist

CTI is seeking a Regulatory Affairs Start-Up professional in Milan to support the RASSU department with submissions, country-specific requirements, and document preparation. You will liaise with Ethics Committees, Competent Authorities, and the CTI Legal team to ensure timely, compliant submissions across country sites. Strong Italian and English, plus...

At Fortrea , we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist , you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will help bring life-changing treatments to...

Study Start Up Associate IIICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and...

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 Clinical Budget Specialist , you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical...

At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist, you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will help bring life-changing treatments to patients...

Fortrea is seeking a Site Start-Up Specialist to coordinate site start-up activities, manage essential documents, and ensure timely regulatory submissions. You will interact with sites, sponsors, and authorities to maintain compliant, audit-ready records. The role requires 2+ years in clinical research or start-up processes, strong ICH/GCP knowledge, and...

Amplifon is the global leader in the hearing care retail industry. Since 1950 we’ve been changing the lives of millions of customers all around the world. And though we are a global company that’s constantly growing, we have a start-up approach and strive for innovation every day. We take pride in setting the standard for our industry and constantly...

At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies. This is an opportunity to lead...

Fortrea is seeking a Site Start-Up Specialist to coordinate site start-up activities, manage essential documents, and ensure timely regulatory submissions. You will work with the FSPx team and collaborate with sponsor sites to advance clinical trials. Ideal candidates have 2+ years in clinical research or regulatory submissions, strong organizational...