... execution Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables ...
The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study ...
... conducted in line with the Study Monitoring Plan (SMP) and will ... no longer active on a study, review and assess training compliance ... external facilities, equipment, and supplies (clinical and non-clinical) continue to be adequate to ...
... and ethical standards of the study. Work closely with clinical, regulatory, and project management teams to ensure Good Clinical Practice (GCP) and regulatory compliance. ...
... manager to support the Medpace Study Start-up group in Europe while being office-based in Munich. This position will be an integral part of the Medpace clinical operations management team. This role ...
... queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: Bachelors degree ...
... you. Responsibilities Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document ...
... deliverables: tracks progress of the clinical trial, manages study data, budget, investigational products, mailings ...
... on time and within study budget. Including but not limited ... (i.e. implementation of study amendment-and changes in study related processes). Reviews and approves ... improvement; training and mentoring of Clinical Trial Administrators, Site Managers and ...
... to information requests related to study indications, disease states, and therapeutic areas, and presenting scientific and clinical data to appropriate audiences. Educating ...