Lead Study Director, GLP & Process Improvement

A leading biopharmaceutical company in Durham, North Carolina is seeking a Study Director to supervise and coordinate client projects. The successful candidate will provide strategic and technical oversight on studies, draft study plans, and ensure compliance with GLP regulations. A Bachelor's degree in a relevant scientific field and 3-5 years of experience are required. The role also requires proficiency in technical writing and data analysis. This position offers opportunities for training and mentorship within a dynamic work environment.
#J-18808-Ljbffr