Senior Clinical Research Associate

Job Summary

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