Study Director — Biocompatibility Studies

Job overview

The Study Director — Biocompatibility Studies role is onsite in South Brunswick Township, NJ, with a Monday–Friday schedule from 9:00 a.m. to 5:00 p.m. and overtime as needed. Compensation is not specified. Eurofins provides analytical testing services intended to help make products, health, and the environment safer. The role directs the technical and regulatory conduct of biocompatibility studies, from protocol development and study oversight through data interpretation and reporting. It also coordinates laboratory operations and staff, maintains sponsor and regulatory-agency communication, and ensures studies follow applicable protocols, SOPs, and GLP requirements.

What you'll do

• Supervise study conduct and technical staff
• develop and implement protocols and experimental designs
• ensure study work follows protocols, SOPs, GLP regulations, and applicable guidelines
• oversee data recording, interpretation, analysis, documentation, and reporting
• coordinate study schedules and track study financial aspects
• train scientists
• liaise with sponsors and regulatory agencies.

What we're looking for

Skills & competencies

study director

biocompatibility studies

south brunswick township nj

eurofins

laboratory operations

regulatory studies

glp

protocol development

data analysis

scientific leadership

monday–friday

9 am–5 pm

overtime as needed

Work arrangement

• Weekend coverage required

About the employer

Eurofins USA BioPharma Services is hiring for this role. Industry: Testing Laboratories and Services. Sector: 54.