Sr Clinical Trial Manager, Clinical Operations

At RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, we blend the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients.

About the role

The Sr Clinical Trial Manager, Clinical Operations is responsible for the oversight, planning, and delivery of assigned clinical study(ies) within the RayzeBio programs. This includes oversight and management of the study Clinical Research Organization (CRO) and Vendors according to corporate and program Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines, and other applicable federal (FDA) and state regulations. The role ensures established study goals are achieved within timelines and budget while maintaining the highest quality.

Responsibilities

• Lead the planning, execution, and closeout of clinical trials from Phase I–III.
• Oversee and manage CROs and vendors to ensure studies 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 study timelines.
• Monitor study progress, including enrollment, site performance, data quality, and key risk indicators; proactively escalate issues to internal stakeholders for timely resolution.
• Identify, assess, and mitigate operational risks; escalate issues as needed.
• Manage study CRO and vendor budgets and invoicing procedures according to study contracts.
• Lead and support country and site feasibility, selection, and activation strategies.
• Actively participate in CRO and vendor meetings; review key operational plans and provide input on operational strategy, including country and site feasibility and start-up.
• Summarize CRO, vendor, and site performance data; escalate study risks to the Clinical Operations Program Lead / Head of Clinical Operations.
• Perform other related duties as assigned.
• Up to 20% travel required.

Requirements

• Minimum 5-7 years of clinical operations experience within biotech, pharma, or CRO industry.
• BA/BS degree, scientific or healthcare discipline preferred.

Skills

• Independent professional who proactively communicates frequently and effectively.
• Detail and action-oriented, organized, and committed to quality and consistency.
• Ability to work successfully in cross-functional teams.
• Ability to work in a dynamic environment with a high degree of flexibility.
• Expertise in Microsoft Project and Smartsheets desired.
• Applies AI to improve team execution and decision-making.

Work Environment

The noise level in the work environment is usually moderate.

Pay

Remote - United States: $149,860 - $181,595 (full-time employee basis). Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate reflects required skills, job location, work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.

Benefits

Eligibility for specific benefits may vary based on job and location. Benefit offerings include:

• Health Coverage: Medical, pharmacy, dental, and vision care.
• Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
• Financial Well-being and Protection: 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.
• Work-life Benefits:
  • Paid Time Off for US Exempt Employees: Flexible time off (unlimited, with manager approval) and 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico, or RayzeBio employees).
  • Paid Time Off for Phoenix, AZ, Puerto Rico, and RayzeBio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays.
  • Additional time off (based on eligibility) may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs, and an annual Global Shutdown between Christmas and New Year’s Day.

Note: All global full- and part-time employees actively employed at and paid directly by BMS at the end of the calendar year are eligible for the Global Shutdown. Summer hours flexibility is available for U.S. office-based employees, with eligibility varying for remote-by-design or lab-based roles.