The Sr. CRA is responsible for monitoring clinical trials to ensure adherence to protocols, regulations, and SOPs while acting as the primary liaison to clinical sites. Key duties include conducting site visits, verifying source data, and contributing to the development of study plans and regulatory reports.
The role involves generating sales to new and existing clients, focusing primarily on selling integrated device design and development services, while also driving sales for regulatory, preclinical, and clinical research aspects. This includes developing sales plans, creating proposals, networking to find leads, and coordinating solutions with internal experts to achieve consistent quarter-over-quarter and year-over-year sales growth.
