Job Description
Caribou Biosciences is seeking a Clinical Trial Manager (CTM) to join our growing Clinical Operations group. You will be responsible for the execution and oversight of clinical trials from start-up through close-out, ensuring alignment with ICH-GCP, applicable regulations, internal SOPs, and protocols. The CTM will collaborate cross-functionally, manage vendors and sites, and contribute to high-quality clinical trial delivery. The CTM will report to the Director of Clinical Operations.
The Clinical Trial Manager will support feasibility assessments, site selection, and study start-up activities, contribute to the development and review of protocols, ICFs, and trial-related documentation, lead creation and maintenance of study trackers, timelines, and study-specific tools, coordinate vendor and site qualification, selection, and onboarding. This role will monitor trial progress and site/vendor performance, review and approve site-specific documents, and manage inventory and logistics. You will proactively identify and mitigate risks, ensure adherence to regulations, and provide timely updates to stakeholders.
About Caribou Biosciences
Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients.