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Clinical Trial Coordinator
hace 2 meses
{"h1": "Clinical Trial Assistant Role at Icon", "p": "At Icon, we are seeking a highly skilled Clinical Trial Assistant to join our team. As a Clinical Trial Assistant, you will play a critical role in ensuring the successful management of clinical trials. Your responsibilities will include partnering with the Global Clinical Trial Manager and Project Manager to ensure overall trial management and adherence to internal SOPs, policies, and local regulatory requirements. You will also support the global study team in performing site feasibility and/or country feasibility, maintain protocol information in Trial Management Systems, and work with the Global Trial Manager & Project Manager to ensure accurate/complete regulatory documents are in place to expedite IEC/IRB or Health Authority approval process. Additionally, you will support the global CTM & PM in collecting and maintaining all documents throughout the trial and post-trial in both eTMF and paper files, distribute, collect, review, and track regulatory documents, agreements, and training documentation, collect and track Financial Disclosure information at appropriate time points, and may contribute to process improvement, including representing functional area in process initiatives and contributing to optimization of daily processes. You may also be assigned as a coach and mentor to a less experienced CTA. Your responsibilities will also include attending Clinical Trial meetings and taking & distributing minutes. ", "h2": "Requirements", "ul": ["Skills set corresponding with preferentially 2+ years relevant clinical trial experience or equivalent", "Relevant systems and tools proficient management (mCTMS, vTMF)", "Proficient in English language", "Strong knowledge with MS Office (Word, Excel, Access, Outlook, Explorer and PowerPoint)", "Strong interpersonal and negotiating skills", "Excellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment"]}
