Study Director - Biocompatibility Studies
Eurofins · South Brunswick Township, NJ
Clinical OperationsFull timeCompany career page
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Role summary
Eurofins seeks a Study Director to oversee biocompatibility research studies and manage laboratory operations. The role involves protocol development, technical supervision, regulatory compliance, and liaison with sponsors and regulatory agencies.
What they're looking for
- Bachelor's degree in animal science, chemistry, biology, microbiology, or related field
- Minimum 5 years experience overseeing biocompatibility studies
- Working knowledge of EPA, FDA, DOT, OECD, GLP regulations and ISO standards
- Hands-on technical knowledge of assigned test procedures
- Strong administrative, leadership, and written communication skills
- Ability to safely wear a respirator
What you'll be doing
- Supervise day-to-day laboratory operations and technical staff assigned to studies
- Develop protocols, experimental designs, and standard operating procedures
- Ensure GLP compliance and proper documentation of all experimental data
- Interpret, analyze, and report study results; maintain sponsor and regulatory agency liaison
- Train and supervise scientists in study procedures and conduct
Privacy & handoff
This role links to Eurofins's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.