Study Director - Biocompatibility Studies
Eurofins USA BioPharma Services · South Brunswick Township
Don’t apply blind. See how your CV matches this role first — free, in 30 seconds.
You will leave NewLuxJob. We do not receive or handle applications.
- Company
- Eurofins USA BioPharma Services
- Location
- South Brunswick Township
- Employment type
- Full-time
- Posted
- October 1, 2026
About this job
Supervise and assist in the conduct of regulatory studies performed. Responsibilities include: Supervise study conduct. Assist in protocol development, design and implementation. Responsibilities as stated in GLP regulations. Data interpretation and report writing. Client liaison. Management Responsibilities: Overall, day-to-day laboratory operation including supervision of technical staff assigned to your studies. Scheduling and coordinating initiation and conduct of studies. Ensure that the study schedule and financial aspects of each study that you are responsible for are accurately tracked on a regular basis. Technical Responsibilities: Overall responsibility for the technical conduct of all studies and interpretation, analysis, documentation and reporting of results.…
This is a short summary.
Want to know if you're a fit? Check your CV against this role — free, in 30 seconds.
Similar jobs
- Part Time Visual Keyholder · COS
- Visual Keyholder · COS
- Director of Product Management, Observability · Elastic
- Consultant - ERP & Supply Chain Systems (EU / LATAM / NA / Asia) · Roundtable on Sustainable Biomaterials
- Agentic-First Software Engineer (Relocate to Miami) · Jiffy
- On-Camera Fitness Instructor · MAGIC
See if your CV fits this job
Paste your CV for an instant match score against this role — and get a tailored cover letter in one click.
- Instant match score for this role
- Tailored cover letter in one click
- Free — no credit card