... Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure ... action plans at site and study level. Supports and completes activities ... Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... card title of Site Management Associate II. Additional responsibilities include: o Site support throughout the study lifecycle from site identification through close-out o ... Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... Prepare and maintain the Investigator Site File and or Trial Master File (TMF) for the study. • Participate in creation and review ... finalization of clinic source documents, time and events tables, and other required study materials; review of Case Report ...
... to the scientific rationale and study criteria of Client’s sponsored studies to specific study sites. Answer medical inquiries, particularly those ... , up to ~50-70% of time About Amplity Amplity Health is ...
... consistency in the management of sites studies Being single point of contact ... or biotech company including site management oversight, clinical study planning and conduct Oncology and ... a reasonable accommodation for any part of the application process, or ...
... the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. ... a reasonable accommodation for any part of the application process, or ...
... at least 60% of the time for future roles is required. • * ... • To assist in coordination of site study related payments, if applicable • *To contact and serve as a contact for clinical sites for basic requests (e.g., ...
... documents and updates for investigator sites, studies, project team, or client • Manages shared mailbox, processes site requests and routes correspondence appropriately • ... Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... , initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring ... at least 60% of the time (international and domestic -fly and ... a reasonable accommodation for any part of the application process, or ...
... initiate and close-out investigational sites for clinical studies in phases II - IV, ensuring ... monitoring experience in medium-sized studies, including study start-up and close-out • ... a reasonable accommodation for any part of the application process, or ...