Study Director

📋 Description

• Supervise study conduct
• Assist in protocol development, design and implementation
• Ensure GLP compliance in all activities
• Data interpretation and report writing
• Client liaison
• Oversee day-to-day laboratory operations and staffing

🎯 Requirements

• BS degree in a related field
• Minimum 5 years' experience overseeing biocompatibility studies
• Strong familiarity with EPA, FDA, DOT, OECD, GLP regulations and ISO standards
• Hands-on knowledge of the tests under responsibility
• Good administrative and leadership skills; effective communication and writing

🎁 Benefits

• Full-time position
• Commutable distance to Dayton, NJ