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Lead Study Director, GLP & Process Improvement

MedPharm Ltd, Durham, NC, United States


A leading scientific research organization in North Carolina is seeking a Study Director to supervise and coordinate client projects. Responsibilities include providing technical oversight, drafting study plans, and adhering to Good Laboratory Practices (GLP). Candidates should have a Bachelor’s degree in a relevant scientific field and 3-5 years of experience. Proficiency in technical writing and data analysis, especially with Microsoft Office, is required. The role allows for up to 5% travel.
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