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