GLP Study Coordinator: Preclinical Research & Compliance

Inside Higher Ed; Philadelphia (Philadelphia County); On-site; USD 70,000 - 90,000; Full time

Job summary

A leading educational organization is seeking a GLP STUDY COORDINATOR to manage non-GLP and GLP preclinical studies involving animal models. The ideal candidate will have 3-5 years of experience in pharmaceutical research, strong technical lab skills, and knowledge of regulatory compliance. This full-time position requires excellent communication and organizational abilities in a fast-paced environment.

Qualifications

• 3-5 years of pharmaceutical/biotechnology experience in GLP studies.
• Solid technical lab skills and ability to maintain records.
• Knowledge of toxicology data generation and review.

Responsibilities

• Coordinate and schedule GLP studies involving animal models.
• Ensure compliance with FDA and GLP regulations.
• Track investigational materials and laboratory records.

Skills

GLP compliance

Technical lab skills

Effective communication

Data analysis

Problem-solving skills

Education

Bachelor’s degree in Chemistry, Biology, Biochemistry

Tools

Microsoft Office

Project management/database software

Job description

A leading educational organization is seeking a GLP STUDY COORDINATOR to manage non-GLP and GLP preclinical studies involving animal models. The ideal candidate will have 3-5 years of experience in pharmaceutical research, strong technical lab skills, and knowledge of regulatory compliance. This full-time position requires excellent communication and organizational abilities in a fast-paced environment.