Regional Clinical Research Associates - Perm positions across the US - (Raleigh, NC)

Position summary Our client, is a specialty CRO that utilizes a broad ability across Women’s Health research with adaptive design and adaptive operational capabilities to deliver medicines and diagnostics of value to women worldwide.They are seeking several experienced CRAs to join their team. They are specifically looking for Northwest, Midwest, Northeast and Southeast metro areas. The CRA will be responsible for performing site monitoring activites for assigned clinical studies in accordance with the Task Order, protocol, standard operating procedures (SOPs), ICH guidelines and all applicable regulatory requirements. Major Assignments include: Responsible for performing on-site monitoring visits to ensure patient safety, GCP compliance and data integrity by confirming the site is conducting the study in accordance with the protocol, ICH guidelines, and applicable regulatory requirements Assists with investigator identification, evaluation and selection activities