Job Description
As a Study Start-Up Associate/Specialist, you will play a pivotal role in the initial phases of clinical trials, ensuring that studies commence efficiently and comply with regulatory standards. Your responsibilities will encompass preparing and submitting essential documents, liaising with ethics committees and regulatory agencies, and ensuring timely site initiation. Collaborating with clinical teams, sponsors, and site personnel, you’ll facilitate the contract negotiation process, address queries related to study start-up, and ensure that sites are equipped and trained to commence the trial. Your meticulous attention to detail and expertise in regulatory requirements will be instrumental in ensuring a smooth and compliant start to clinical research projects, setting the foundation for their successful execution.
