Sr. Clinical Research Associate

Conduct ongoing study monitoring including frequent periodic site visits, protocol adherence checks, and material handling procedures for assigned clinical trials. Participate in study design by assisting with protocol and case report form preparation, while generating clinical SOPs, policies, and plans per US and international guidelines. Initiate studies through site visits, supply shipments, and procurement of budgets, contracts, and regulatory documents. Prepare site visit reports detailing key accomplishments, issues, and follow-up recommendations, and conduct termination visits to obtain final reports for regulatory submission. Maintain clinical archives and electronic files. Requires BA/BS degree, 5+ years clinical research experience, and adherence to GCPs.