Clinical Research Associate 1

Design and prepare clinical protocols and case report forms, then generate SOPs, policies, and plans adhering to US and international guidelines. Evaluate potential clinical sites and initiate studies by performing site visits, arranging supply shipments, and conducting ongoing monitoring including periodic checks, protocol adherence reviews, and file inspections. Prepare site visit reports with key accomplishments and recommendations, manage procurement of budgets and regulatory documents, and conduct termination visits to obtain final reports for regulatory submission. Maintain clinical archives and electronic files while assisting with study documentation. Requires a BA, BS, RN, or BSN with basic GCP knowledge and 1-2 years of clinical research experience.