Clinical Research Associate - (Apex, NC)

Senior Clinical Research Associate (Senior CRA) The Senior CRA will monitor activities at clinical sites to assure adherence to Good Clinical Practices, SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. The successful CRA must be able to work both independently and in a team environment. Identify, select, and monitor investigational sites for clinical studies Track progress of study including patient enrollment and monitoring visits Investigate queries and monitor discrepancies Manage the site conduct, and the investigational product accountability and reconciliation process Negotiate and manage the budget and payments for investigative sites and contract organizations Design and administer case report forms (CRFs) Prepare clinical protocols, amendments, consent forms, study guides, CRFs, and any other clinical research related document