Director – Global Oncology Clinical Research

Responsible for directing the following activities for assigned clinical drug studies. Directs the design, development, and execution of clinical drug development plans, protocols and related activities. Assures that protocols will adhere to standard clinical practices. Designs protocols from a physician’s standpoint. Secures the conditions essential for safety, efficacy, and medical usefulness of a drug. Decides how the resulting data should be analyzed and interpreted. Recommends new approaches to data analysis and preparation. Develops staff of physicians, scientists, and coordinators by providing training and guidance. Organizes meetings to discuss critical issues, such as safety and efficacy. Participates in Project Development Teams. Coordinates with related clinical functional areas such as Biostatistics, Human Pharmacology and Regulatory Affairs.

Education Requirements:   MD degree, board certified/board eligible