Senior Clinical Research Associate

Job Summary

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