Study Start-Up Specialist, IQVIA Biotech, United Kingdom

Job description

Regulatory & Start-Up Specialist, IQVIA Biotech, UK Homebased: IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster. Job Overview: We are seeking a highly motivated Regulatory & Start-Up Specialist to support clinical trial site activation activities across the UK. In this role, you will play a pivotal part in ensuring studies are initiated efficiently, compliantly, and in alignment with regulatory requirements, SOPs, and project timelines. You will collaborate cross-functionally and act as a key liaison between sites, project teams, and internal stakeholders, contributing to the successful delivery of clinical trials. Key Responsibilities: Act as the Single Point of Contact (SPOC) for assigned studies, supporting investigative sites, Site Activation Managers (SAMs), Project Management, and internal teams Deliver site start-up and activation activities in compliance with local and international regulations, SOPs, and work instructions Prepare and review regulatory documentation, ensuring compl...