Experienced Clinical Research Associate, Italy
Your responsibilities will include:
Performing site selection, initiation, monitoring and close-out visitsSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representatives
Qualifications:
University Bachelor's Degree and Master's Degree in scientific discipline or health careIn possession of CRA Certification as required by Ministerial Decree dated 15.11.2011Experience in Pharma Industry, and/or Clinical Trials environmentVery good computer skills including MS...