Consultant; 1099/W2 contract and project-based assignment. Clinical Program Director, Clinical Trial Manager, Real-World Evidence, Ad-hoc projects. Clinical research professional with extensive experience in clinical trial operations/management, GCP compliance and process development with an emphasis in CNS, Gastrointestinal, and Oncology therapeutic areas. Brings 24 years of experience in global Phase I-IV drug and device trials and registries, including 18 years of project management, 2 years of data operations, and 3 years of monitoring experience. Applies strong analytical, leadership, and communication skills as well as a solid working knowledge of clinical research standards, regulations and best practices.