Senior Clinical Research Associate

Responsible for monitoring phase I through phase IV clinical research studies and Real World Evidence (RWE) studies, the full-time Senior Clinical Research Associate will manage site activities, conduct site visits, and ensure compliance with regulatory guidelines while working remotely. Key responsibilities Serve as the main contact for assigned study sites and conduct various site visits, ensuring adherence to regulatory requirements and timelines Assist with study start-up activities, including feasibility assessments and site selection, while managing essential regulatory documents Implement subject enrollment strategies and provide ongoing updates of site status to the Clinical Project Manager Required qualifications At least 1 year of clinical trial monitoring experience or equivalent experience as determined by management Bachelor's Degree or higher in an allied health field, or equivalent experience in nursing or related areas Previous experience in conducting clinical research studies in a hospital, pharmaceutical company, or CRO Demonstrated successful performance in a CRA position with a minimum of 1 year of on-site monitoring experience preferred Virtual Vocations Inc