This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Study Start Up Specialist based in Brazil. We are seeking a detail-oriented and proactive professional to support the successful initiation of clinical trials. In this role, you will coordinate essential study start-up activities, helping ensure clinical sites are activated efficiently and in compliance with regulatory requirements. You will collaborate with global study teams, regulatory stakeholders, and site personnel to facilitate documentation, submissions, and approvals. Your work will contribute to accurate project tracking, effective communication, and timely delivery of study milestones. This opportunity offers a collaborative, international environment where organizational skills and clinical research expertise make a meaningful impact. If you are passionate about clinical trial operations and advancing medical research, this role offers an opportunity to contribute to the development of potentially life-changing therapies.