Job Description
As a Study Start-Up Manager, you will lead and coordinate the initial phases of clinical trials, ensuring a streamlined and compliant commencement of studies. Your role will involve overseeing the preparation and submission of essential documents, managing interactions with ethics committees and regulatory bodies, and ensuring timely site initiation across multiple locations. Collaborating with cross-functional teams, you’ll drive the contract negotiation process, develop start-up strategies, and ensure that all sites are adequately trained and equipped to begin the trial. Your leadership and expertise in the start-up phase will be crucial in mitigating potential delays, ensuring regulatory compliance, and setting the stage for the successful execution of clinical research projects.
