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.