Clinical Research Associate I

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