Clinical Trial Manager, Clinical Operations
Bristol Myers Squibb
August 22, 2026
Remote
United States
Clinical Research and Development
Clinical Trial Manager, Clinical Operations
Responsibilities:
- Lead planning, execution, and closeout of clinical trials (Phase I–III).
- Oversee and manage CROs and vendors to ensure studies are on time, within budget, and compliant with RayzeBio SOPs, FDA regulations, and ICH/GCP.
- Lead cross-functional study execution team to achieve goals and deliverables.
- Plan and execute study timelines.
- Monitor progress (enrollment, site performance, data quality, key risk indicators); proactively escalate issues for timely resolution.
- Identify, assess, and mitigate operational risks; escalate as needed.
- Manage CRO/vendor budgets and invoicing per study contract.
- Lead/support country and site feasibility, selection, and activation.
- Participate in CRO/vendor meetings; review operational plans and provide input.
- Summarize CRO/vendor/site performance and escalate study risks to Clinical Operations leadership.
- Up to 20% travel.
Qualifications (Education/Experience):
- 5–7 years clinical operations experience in biotech/pharma/CRO.
- BA/BS degree in scientific or healthcare discipline (preferred).
Skills/Requirements:
- Proactive, effective communication.
- Detail-oriented, organized, quality-focused.
- Ability to work in cross-functional teams.
- Flexibility in dynamic environments.
- Microsoft Project and Smartsheet expertise desired.
- Applies AI to improve execution and decision-making.
Compensation/Benefits (as stated):
- Remote (US): $134,505–$162,988.
- Benefits include medical/dental/vision; wellbeing support; 401(k) and insurance/disability.
- Paid time off (flexible time off or annual vacation depending on location/role).
Responsibilities:
- Lead planning, execution, and closeout of clinical trials (Phase I–III).
- Oversee and manage CROs and vendors to ensure studies are on time, within budget, and compliant with RayzeBio SOPs, FDA regulations, and ICH/GCP.
- Lead cross-functional study execution team to achieve goals and deliverables.
- Plan and execute study timelines.
- Monitor progress (enrollment, site performance, data quality, key risk indicators); proactively escalate issues for timely resolution.
- Identify, assess, and mitigate operational risks; escalate as needed.
- Manage CRO/vendor budgets and invoicing per study contract.
- Lead/support country and site feasibility, selection, and activation.
- Participate in CRO/vendor meetings; review operational plans and provide input.
- Summarize CRO/vendor/site performance and escalate study risks to Clinical Operations leadership.
- Up to 20% travel.
Qualifications (Education/Experience):
- 5–7 years clinical operations experience in biotech/pharma/CRO.
- BA/BS degree in scientific or healthcare discipline (preferred).
Skills/Requirements:
- Proactive, effective communication.
- Detail-oriented, organized, quality-focused.
- Ability to work in cross-functional teams.
- Flexibility in dynamic environments.
- Microsoft Project and Smartsheet expertise desired.
- Applies AI to improve execution and decision-making.
Compensation/Benefits (as stated):
- Remote (US): $134,505–$162,988.
- Benefits include medical/dental/vision; wellbeing support; 401(k) and insurance/disability.
- Paid time off (flexible time off or annual vacation depending on location/role).