Senior Clinical Research Associate

To ensure successful protocol level execution of clinical studies, the full-time remote Senior Clinical Research Associate will manage site-related study execution, including monitoring visits, site evaluations, and adherence to regulatory standards. Key responsibilities Oversee site monitoring activities, including selection, activation, and close-out processes Ensure compliance with federal regulations, Good Clinical Practices (GCP), and AbbVie Standard Operating Procedures (SOPs) Coach and mentor Clinical Research Associates (CRAs) while maintaining audit readiness for assigned sites Required qualifications Bachelor's degree or equivalent in a health-related field (e.g., Medical, Scientific, Nursing, Pharmacy) preferred Minimum of 3 years of site monitoring experience Strong analytical and critical thinking skills for complex issue evaluation Excellent interpersonal skills with a persuasive communication style Demonstrated planning and organizational skills with flexibility in a dynamic environment