The role involves performing and coordinating all aspects of clinical monitoring and site management, including conducting remote or on-site visits to assess compliance with protocols and regulations. Responsibilities include acting as a site processes specialist to ensure trials adhere to guidelines, guaranteeing subject rights, well-being, and data reliability.

The primary responsibility involves building Epic workflows specifically for CPACS integration to support recent acquisitions across the state. This role requires extensive build experience within the Epic Cupid module.

The Medical Science Liaison acts as a field-based medical expert, supporting ARS products by fostering scientific relationships and exchanging knowledge with healthcare communities and internal stakeholders to optimize patient outcomes. This role involves educating internal and external parties on product science and supporting the generation of medical-scientific knowledge through subject matter expertise.

Clinical Scientist Associate Director managing late-phase clinical development at Amgen