Description

You coordinate high throughput early discovery assays and monitor nonclinical toxicology studies conducted at CROs.

Responsibilities

• Coordinate high throughput early discovery assays following templated work instructions.
• Collaborate with internal research departments and multi-site CROs to ensure timely data and report uploads.
• Perform QC review of nonclinical regulatory documents, data tables, study protocols, and reports.
• Manage study monitoring for nonclinical toxicology studies to ensure technical and scientific conduct.
• Assist with administrative tasks and document management as required.

Required Skills

• 1+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development.
• BS or BA degree in a scientific discipline.
• Proficiency in Microsoft Excel, Word, and PowerPoint.
• Experience with QC review of regulatory documents and study protocols.
• Ability to prioritize multiple tasks, plan proactively, and meet deadlines.
• Strong attention to detail and quality of work.

Preferred Skills

• MS degree with 3+ years of pharmaceutical or CRO industry experience or BS degree with 5+ years.
• Knowledge of general principles and methods of toxicology, animal and human biology, and physiology.

Key Skills

Education

Any Gradute