Study Coordinator
Inotiv
September 06, 2026
Full-time
On-site
Westminster, CO
Clinical Research and Development
Role: Study Coordinator supporting preclinical research in a biopharma setting, focusing on in-life animal studies within regulated environments. Responsibilities: manage study initiation, coordinate sample and material logistics, ensure protocol adherence, review and document raw data, prepare study files, and support study conduct and amendments. Maintain compliance with GLPs, USDA, OLAW, AAALAC, and SOPs; perform quality checks; and assist in regulatory and study documentation processes. Requirements: Bachelor's in life sciences or related field; minimum 3 years relevant pharmaceutical or research experience; at least 1 year animal handling experience; proficiency in lab procedures, document review, and computer applications. Skills: detail-oriented with strong communication, problem-solving, and collaborative abilities; capable of working in regulated environments and following CFR protocols. High-Value: preclinical animal studies, laboratory compliance, GLP standards, protocol development, and data review. Work setup: primarily office/lab environment; physical activity includes moderate lifting and PPE usage; schedule may be flexible.