What are the responsibilities and job description for the ASSOCIATE, CLINICAL TRIAL position at Idaho State Job Bank?
Associate, Clinical Trial at Sumitomo Pharma in Boise, Idaho, United States Job Description Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in the U.S., Canada, and Europe, a diverse pipeline of early- to late-stage assets, and in-house advanced technology capabilities, we aim to accelerate discovery, research, and development to bring novel therapies to patients sooner. For more information on SMPA, visit our website (or follow us on LinkedIn (. Job Overview We are currently seeking a dynamic, highly motivated, and experienced individual for the position of Clinical Trail Associate. The Clinical Trial Associate (CTA) will be responsible for supporting the conduct of clinical trials and handling administrative aspects of clinical trial execution. This role will support completion of all study deliverables, ensuring the highest level of data quality; proactively identifies, communicates, and resolves clinical study operational issues; and participates in process improvement initiatives as required. This role adheres to Clinical Standard Operating Procedures and Good Clinical Practice ICH Guidelines. Job Duties and Responsibilities Perform general administrative tasks to support team members with clinical trial execution, e.g., development and formatting of documents, review and reconciliation of study- specific information, etc. Assist in maintaining study status updates on a weekly basis (e.g., IRB approvals, regulatory document collection, patient enrollment, monitoring status, etc.) Track and prepare study-specific information using databases, spreadsheets, and other tools Review and / or approval of study documentation, including essential document packets, study plans, informed consent forms, etc. Manage clinical and non-clinical supplies, including purchase and shipping Help with the development and distribution of site binders Set-up and coo To view full details and how to apply, please login or create a Job Seeker account
