When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Job Summary: The Clinical Trial Specialist (CTS) is responsible for assisting with study management of assigned projects in accordance with SOPs, Good Clinical Practice (GCP), International Conference of Harmonization (ICH) guidelines and local regulations. Study management activities may include maintenance of information databases and trial tracking reports, coordination of clinical trial documentation and general support to ensure the successful and timely execution of clinical activities and deliverables. Key Accountabilities: Develop, organize and maintain tracking systems and tools across multiple programs to support efficient execution, oversight and compliance of a clinical study from start-up to closeout Coordinate and lead the development, review and maintenance of study management tools, monitoring tools, study manuals and training materials and presentations Schedule meetings, coordinate and distribute meeting agendas, minutes, and follow-up action items for study teams. Establish, manage and oversee study files and shared spaces to ensure accuracy, accessibility and compliance Manage documentation of study training to ensure compliance Manage study sample and supply accountability and develop collaborative relationships with vendor teams. Partner with the study management team to Lead or manage specific projects as appropriate. Serve as a key point of contact for study team members, facilitating effective communicati
