• 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...