Study Director

📋 Description Supervise and assist in the conduct of regulatory studies. Assist in protocol development, design and implementation. Responsibilities as stated in GLP regulations. Data interpretation and report writing. Client liaison. Overall day-to-day laboratory operation including supervision of technical staff. 🎯 Requirements PhD or equivalent in related field. Familiarity with EPA, FDA, DOT, OECD, GLP regs and ISO standards. Hands-on knowledge of the tests under responsibility. Strong administrative and leadership skills; effective communication. 🎁 Benefits Full-time position with standard business hours. Overtime as needed. Commutable distance to Dayton, NJ encouraged.