/ http://www.slideshare.net/images/logo.gif / ºÝºÝߣShare feed for ºÝºÝߣshows by User: khajak https://cdn.slidesharecdn.com/profile-photo-khajak-48x48.jpg?cb=1666117058 • Manage multi-site national/international phase I-III clinical trials • Allocation of personnel and financial resources to the projects based on the project plans • Provide leadership in developing educational study-related documents, including contracts • Responsible for regulatory, legal and organizational policy compliance requirements and file documentation • Coordinate and review laboratory, clinical SOPs, protocol and ICF development. • Manage programming of eCRF pages • Expenditure review and analysis to ensure sponsor compliance • Improve efficiency of the clinical trial project management using processes as measured by reduction in throughput time. • Impleme... http://www.business.pitt.edu/about/ebl/mckinsey-cup.html