Senior Study Director, Nonclinical Toxicology (GLP)

NorthernBio; Muskegon (MI); On-site; USD 90,000 - 150,000; Full time

Job summary

NorthernBio in the United States seeks a Research Scientist/Study Director to lead non-clinical studies under GLP, ensuring study integrity and regulatory compliance. You will act as the single point of control for study planning, execution, data collection, and reporting.

The ideal candidate has 5–7 years in the CRO industry as a Toxicologist, with strong experience in study design, data analysis, and scientific writing. Excellent communication and attention to regulatory detail are essential.

Qualifications

• Master’s degree or equivalent in a related discipline; PhD preferred.
• 5 years GLP-compliant lab experience preferred.
• Experience with peer-reviewed publications and scientific writing.
• Proficiency with Microsoft Office and ability to learn new applications.
• Excellent written and oral communication skills.
• Knowledge of GLPs (FDA, OECD, and MHLW) and other federal regulations relating to the care of laboratory animals.

Responsibilities

• Serve as Study Director for non-clinical studies and control overall planning.
• Conduct data interpretation, analysis, documentation, and reporting of results.
• Generate protocol and ensure protocol changes are approved and followed.
• Ensure all raw data, documentation, and final reports are archived.
• Interface with Sponsors, Vendors, Contributing Scientists and Principal Investigators.
• Other duties as assigned.

Skills

GLP Compliance

Study Design

Data Analysis

Scientific Writing

Communication Skills

Education

Master’s Degree or equivalent in a related discipline

PhD preferred

Job description

NorthernBio in the United States seeks a Research Scientist/Study Director to lead non-clinical studies under GLP, ensuring study integrity and regulatory compliance. You will act as the single point of control for study planning, execution, data collection, and reporting.

The ideal candidate has 5–7 years in the CRO industry as a Toxicologist, with strong experience in study design, data analysis, and scientific writing. Excellent communication and attention to regulatory detail are essential.