Clinical Research Associate 1 - CFSP

Clinical Research Associate Your responsibilities will include: Performing site selection, initiation, monitoring and close-out visits after completing training period Supporting the development of a subject recruitment plan Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions Collaborating with experts at study sites and with client representatives Qualifications: University degree in scientific discipline or health care At least 6 moths of experience in Pharma Industry, and/or Clinical Trials environment Very good computer skills includi…