Job Overview
Location
Remote - United States - US
Job Type
Full-time
Category
DevOps
Date Posted
June 6, 2026
Full Job Description
đź“‹ Description
- • Lead the planning, execution, and closeout of clinical trials from Phase I to Phase III for RayzeBio programs.
- • Oversee and manage Clinical Research Organizations (CROs) and vendors to ensure trials are completed on time, within budget, and in compliance with RayzeBio SOPs, FDA regulations, and ICH/GCP guidelines.
- • Lead cross-functional study execution teams to achieve study goals and deliverables.
- • Plan and execute detailed study timelines, monitoring progress including patient enrollment, site performance, data quality, and key risk indicators.
- • Proactively escalate operational issues to internal stakeholders to ensure timely resolution and maintain trial integrity.
- • Identify, assess, and mitigate operational risks associated with clinical trials and escalate critical concerns to the Clinical Operations Program Lead or Head of Clinical Operations.
- • Manage CRO and vendor budgets and invoicing procedures in alignment with study contracts.
- • Lead or support country and site feasibility assessments, selection, and activation strategies for clinical trials.
- • Actively participate in CRO and vendor meetings, reviewing operational plans and providing strategic input on country and site start-up activities.
- • Summarize performance data from CROs, vendors, and clinical sites to inform program-level decisions and risk management.
- • Perform other related duties as assigned, ensuring adherence to regulatory and corporate standards.
- • Travel up to 20% as required for site visits, meetings, and trial oversight.
🎯 Requirements
- • Minimum 5-7 years of clinical operations experience within biotech, pharma, or CRO industry
- • BA/BS degree in a scientific or healthcare discipline preferred
- • Expertise in Microsoft Project and Smartsheets desired
- • Independent professional with proactive and effective communication skills
- • Detail and action-oriented with strong organizational skills and commitment to quality and consistency
- • Ability to work successfully in cross-functional teams and in a dynamic, flexible environment
🏖️ Benefits
- • Medical, pharmacy, dental, and vision care coverage
- • Wellbeing support programs including BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP)
- • 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support
- • Paid Time Off: US Exempt Employees receive flexible time off (with manager approval) and 11 paid national holidays; Phoenix, AZ, Puerto Rico, and RayzeBio employees receive 160 hours annual paid vacation, 11 national holidays, and 3 optional holidays
- • Unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility (for eligible US office-based employees), and leaves for medical, personal, parental, caregiver, bereavement, and military needs
- • Annual Global Shutdown between Christmas and New Year’s Day for all eligible global employees
Skills & Technologies
About Bristol-Myers Squibb Company
Bristol-Myers Squibb is a global biopharmaceutical company headquartered in New York City. It discovers, develops, manufactures and markets medicines for cancer, cardiovascular, immunologic, fibrotic and infectious diseases. Formed through the 1989 merger of Bristol-Myers and Squibb, the company has pioneered therapies such as Opdivo, Yervoy and Eliquis. Operating in more than 60 countries, it invests heavily in R&D and partnerships to advance precision oncology, cell therapy and immunotherapy. BMS acquired Celgene in 2019, expanding its oncology and hematology portfolio. The company is committed to sustainability, access to medicines and global health equity initiatives.
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