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Responsibilities:
- Manage operational activities for all phases of clinical studies, including start-up, maintenance, and close-out.
- Provide sponsor oversight of CROs and vendors to ensure compliance and quality.
- Collaborate cross-functionally on trial timelines, budgets, and documentation.
Requirements:
- BS with 6+ years in Clinical Operations or MS with 4+ years; 3 years Sponsor CTM experience.
- Experience with complex global Phase III trials, cell therapy or oncology.
- Proficiency in ICH-GCP, FDA, EMA regulations, and Microsoft 365.
Compensation & Benefits:
- Competitive salary, bonus, and equity for all employees.
- Generous paid vacation, medical, dental, vision insurance, and 401(k) matching.
- Employee stock purchase plan and tuition reimbursement.
Caribou Biosciences
Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company developing off-the-shelf cell therapies for devastating diseases. The company fosters an open, collaborative culture where diverse perspectives are welcomed, with teams working from Berkeley or remotely.