Bristol Myers Squibb · 1 day ago
Director, Clinical Site Operations
United States
Full-time
Onsite
Director/Executive
$211K/yr - $255K/yr
10+ years expBristol Myers Squibb is a dynamic biotechnology company dedicated to transforming patients' lives through innovative treatments. The Director, Clinical Site Operations provides strategic oversight and management of clinical trial execution, ensuring compliance with corporate goals and regulatory guidelines while maintaining high quality and efficiency in operations.
BiotechnologyHealth CareMedicalPharmaceuticalPrecision Medicine
Responsibilities
Directs the operational oversight and execution of clinical site start-up, management and monitoring in accordance with RayzeBio SOPs, ICH Guidelines, and Good Clinical Practices (GCP) to ensure overall data quality, integrity, and patient protection and safety
Manages CRO relationship and oversight to ensure the appropriate scope of work, oversight and training of the clinical team, investigators and site staff as well as the achievement of study milestones within agreed upon timelines and budget
Develops collaborative relationships with investigative sites
Communicates clinical site performance data to the Head of Clinical Operations and the Clinical Program Management team
Key contributor to the development, review and approval of study documents including but not limited to RayzeBio SOPs and Clinical Operation Plans
Liaison with other functional departments to ensure that the highest quality is maintained
Participate in and/or lead departmental initiatives
Line management skills and expertise in mentoring and coaching
Detail oriented, organized and committed to quality and consistency
Excellent team-interaction skills and ability to work successfully in cross-functional teams
Ability to work in a dynamic environment with a high degree of flexibility
Represent RayzeBio at conferences as well as scientific and other business-related meetings as required
Assists in creating vision for department goals and objectives
Conduct oversight visits at investigational sites to ensure quality monitoring
Up to 20% travel required
Qualification
Required
Minimum 10 years clinical operations experience within biotech, pharma or CRO industry
Proven experience in clinical research as team lead in clinical functions
BA/BS degree, scientific or healthcare discipline preferred
Directs the operational oversight and execution of clinical site start-up, management and monitoring in accordance with RayzeBio SOPs, ICH Guidelines, and Good Clinical Practices (GCP) to ensure overall data quality, integrity, and patient protection and safety
Manages CRO relationship and oversight to ensure the appropriate scope of work, oversight and training of the clinical team, investigators and site staff as well as the achievement of study milestones within agreed upon timelines and budget
Develops collaborative relationships with investigative sites
Communicates clinical site performance data to the Head of Clinical Operations and the Clinical Program Management team
Key contributor to the development, review and approval of study documents including but not limited to RayzeBio SOPs and Clinical Operation Plans
Liaison with other functional departments to ensure that the highest quality is maintained
Participate in and/or lead departmental initiatives
Line management skills and expertise in mentoring and coaching
Detail oriented, organized and committed to quality and consistency
Excellent team-interaction skills and ability to work successfully in cross-functional teams
Ability to work in a dynamic environment with a high degree of flexibility
Represent RayzeBio at conferences as well as scientific and other business-related meetings as required
Assists in creating vision for department goals and objectives
Conduct oversight visits at investigational sites to ensure quality monitoring
Up to 20% travel required
Benefits
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.
Paid Time Off
US Exempt Employees flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
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
Eligibility for specific benefits listed on our careers site may vary based on the job and location.
Company
Bristol Myers Squibb
At Bristol Myers Squibb, we work every day to transform patients’ lives through science.
10001+ employees
H1B Sponsorship
Bristol Myers Squibb has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (247)
2024 (278)
2023 (231)
2022 (180)
2021 (181)
2020 (169)
Funding
Current Stage
Public CompanyTotal Funding
$29.32BKey Investors
Venrock
2025-11-05Post Ipo Debt· $5.74B
2024-02-14Post Ipo Debt· $13B
2023-10-30Post Ipo Debt· $4.5B
Leadership Team
Charles Bancroft
CFO
Cristian Massacesi
Executive Vice President, Chief Medical Officer and Head of Development
Recent News
2026-01-23
Company data provided by crunchbase