Clinical Research Associate

Conduct ongoing study monitoring including frequent periodic site visits, protocol adherence checks, material handling procedures, and inspection of study files. Prepare site visit reports identifying key accomplishments, issues for resolution, and recommendations for follow-up actions. Participate in the evaluation of potential clinical sites, initiate studies by performing initiation site visits, and arrange for shipment of clinical supplies and case report forms. Generate clinical SOPs, policies, charters, and plans according to US and international guidelines. Assist in the design and preparation of protocols and case report forms, procure budgets and contracts, and conduct study termination visits to obtain final reports from investigators. Maintain clinical archive and electronic files. Requires a BA, BS, RN, or BSN with 3+ years of clinical research experience and adherence to GCPs.