Clinical Research Associate I

Job Summary

To support clinical research excellence, the full-time Clinical Research Associate I will engage with investigative sites in Little Rock, Arkansas, Memphis, Tennessee, and Shreveport, Louisiana, ensuring compliance with trial protocols and enhancing data integrity while working remotely.

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 compliance with regulations and quality standards
• Implement site engagement strategies and monitor overall study performance, addressing any risks or issues proactively

Required qualifications

• Bachelor's degree or equivalent, preferably in a health-related field (e.g., Medical, Scientific, Nursing, Pharmacy)
• Clinically related experience, ideally in clinical research coordination or data management
• Understanding of therapeutic area indications and scientific concepts related to clinical trials
• Knowledge of regulatory requirements, ICH/GCP Guidelines, and applicable policies
• Strong interpersonal skills with the ability to build relationships and collaborate effectively across teams