Jennifer Huttenburg, MS

Vice President, Compliance & Operations | GCP QA Lead

Jennifer Huttenburg, MS, has over 17 years of Clinical Operations and GCP Compliance experience in the biotech industry. She has expertise in managing all aspects of clinical study conduct from Trial Master Files to Vendor Management and Study Team Leadership. Jennifer has worked on all stages of clinical studies from early phase to large international, registrational studies. In addition to her Clinical Operations experience, she has supported Quality Management System (QMS) development for small companies and enjoys working with teams on GxP related compliance activities.

Most of Jennifer’s experience has been working with small biotech companies which has given her a vast understanding of what goes into running clinical studies and maintaining GxP compliance in a small company setting.