Clinical Research Associate I

Job Summary

To advance clinical research initiatives, the full-time Clinical Research Associate I will manage site engagements, ensure compliance with trial protocols, and drive data integrity while working remotely and covering territories in Little Rock, Arkansas, Memphis, Tennessee, and Shreveport, Louisiana.

Key responsibilities:

• Serve as the primary contact for investigative sites, providing information on clinical trials and fostering partnerships
• Conduct site evaluations, training, and monitoring activities to ensure adherence to protocols and regulatory standards
• Implement site engagement strategies and assess recruitment and retention techniques to enhance study performance

Required qualifications:

• Bachelor's degree or equivalent, preferably in a health-related field (e.g., Medical, Scientific, Nursing, Pharmacy)
• Clinical research coordinating or data management experience
• Knowledge of therapeutic area indications and regulatory requirements, including ICH/GCP Guidelines
• Ability to work collaboratively and develop relationships across functions
• Strong planning and organizational skills to manage multiple projects effectively