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 monitoring activities, oversee compliance with regulatory standards, and mentor Clinical Research Associates.

Key responsibilities

• Manage start-up, execution, and close-out of clinical trials at assigned sites, including monitoring visits and site evaluations
• Ensure adherence to federal regulations, Good Clinical Practices (GCPs), and AbbVie Standard Operating Procedures (SOPs) while maintaining audit readiness
• Coach and mentor Clinical Research Associates, providing input on their development and training needs

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 evaluating complex issues
• Excellent interpersonal skills with the ability to communicate effectively and adapt to changing requirements
• Demonstrated planning and organizational skills with a high level of flexibility in a dynamic environment