... execution Responsible for management of study vendor Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables ...
... support in contract negotiations with clinical trial sites, CROs and vendors Creation of study concepts, plans and reports as ...
... 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 ...
... 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 ...
... you. Responsibilities Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document ...
... 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 ...
... to information requests related to study indications, disease states, and therapeutic areas, and presenting scientific and clinical data to appropriate audiences. Educating ...
... to information requests related to study indications, disease states, and therapeutic areas, and presenting scientific and clinical data to appropriate audiences. Educating ...
... the future of clinical development. As a Clinical Research Associate II at ICON, ... responsibility for study cost efficiency Preparation and review of study documentation and feasibility studies for ... sized studies, including study start-up and close-out ...