Provide leadership and coordination with key research functions to one or more drug development programs.
Lead development of the Clinical Strategy/Clinical Development Plan and provide medical oversight into protocol development, study conduct and data generation, as well as reporting.
Lead and coordinate study activities in the program.
Oversee Phase I-III clinical development programs to ensure that regulatory requirements and quality standards are met. Strive to maintain or exceed compliance obligations for Good Clinical Practices guidelines and standard company operating procedures.
Be a company representative interacting with external scientific leaders and regulatory authorities for assigned program(s).
Search and analyze medical literature to write and review abstracts, manuscripts for publications or presentation internally and externally