Ref #: 28929

Employment type: Permanent - Full-Time

Location: US-New York

Posted: 07-May-2021


• The Clinical Research Associate is regionally based and is responsible for the monitoring of clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines and company SOPs, to support New Drug Applications. The CRA will support project teams in the placement, implementation, communication, site management, recruitment and retention issue identification and resolution, and activities required at the conclusion of clinical studies, as stipulated in the monitoring plans for assigned projects. The CRA will expand his/her responsibilities as directed by the Clinical Research Manager or Clinical Project Leader to include fostering the development of the monitoring program and/or facilitating the objectives of the clinical project teams. The CRA will also assist the CRM/CPL, as directed, in the training, mentoring and supervision of CRAs, assisting in co-monitoring of sites and in completing special projects and assignments to further advance the monitoring program and its contributions to the clinical research department.