• Responsible for managing the activities of several global clinical studies including assisting in the development of study-related documents, study site management, and patient data monitoring. • Provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance. • Assist Clinical Project Manager in the development and management of company-sponsored global clinical trials • Lead in reviewing completed assignments by members of the clinical development group • Lead/assist in the development and management of revisions to study-related documents such as the informed consent, laboratory manual, pharmacy manual, case report forms (CRFs) and other study execution tools. • Provide support in site recruitment, site initiation, site payments and site close-out. • Help to oversee the training of new clinical site staff or site training for protocol amendments. • Liaise with the in-house team to ensure collection of updated regulatory documents as needed. • Help to provide guidance to clinical sites on a daily basis including protocol interpretation and protocol safety compliance. • Lead/Assist in the training of clinical development group staff. • Assist CPM to prepare and update clinical trial updates for Clinical Development team • Provide support for summarizing and maintaining patient treatment, response and survival data for active studies. • Other duties as assigned