Senior Clinical Trial Manager, Clinical Operations

Bristol Myers Squibb

. Manage study vendors, including Central Lab, RTSM/IRT, Imaging, and Dosimetry Vendors .

Posted 10/8/2026full-timeRemote • United StatesSenior💰 $119,116 - $144,341 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical study vendors and ensuring compliance with FDA regulations and ICH/GCP guidelines. Proficient in developing operational plans and risk mitigation strategies while effectively communicating and collaborating within cross-functional teams.

Highest-signal resume keywords

Clinical Operations ExperienceVendor ManagementRisk Mitigation StrategiesMicrosoft Project ExpertiseCross-Functional Team Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study Protocol ReviewVendor Performance MetricsStudy Documentation ManagementBudget ManagementInformed Consent Form Review

Soft Skills

Proactive CommunicationDetail-OrientedOrganizational SkillsFlexibilityCommitment to Quality

Tools & Technologies

Microsoft ProjectSmartsheetsAI Tools

Industry Keywords

BiotechPharmaCROFDA RegulationsICH/GCP Guidelines

About the role

Key responsibilities & impact

Manage study vendors, including Central Lab, RTSM/IRT, Imaging, and Dosimetry Vendors
Ensure vendor deliverables are on time, within budget, and compliant with RayzeBio SOPs, FDA regulations, and ICH/GCP guidelines
Participate in vendor meetings
Develop and manage vendor study operational plans
Develop and manage risk mitigation strategies
Review key performance indices and vendor metrics
Assist the Study Lead with management of the study CRO
Review Clinical Study Protocol, Informed Consent Forms, study documents, and plans
Participate in CRO and Study Execution Team meetings
Provide input to operational strategy, including study and country start-up
Support site feasibility, selection, initiation, and issue resolution
Track and maintain study documentation, including TMF completeness and quality
Monitor and report study vendor progress
Escalate issues and study risks to internal stakeholders and the Study Lead
Assist with study vendor budgets and invoicing procedures
Summarize vendor performance data
Perform other related duties as assigned

Requirements

What you’ll need

Minimum 2-3 years clinical operations experience within biotech, pharma or CRO industry
BA/BS degree in a scientific or healthcare discipline preferred
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
Uses AI tools to enhance individual productivity and quality of work
Up to 10% travel required

Benefits

Comp & perks

Additional discretionary incentive cash
Stock opportunities
Wellbeing support
Retirement and financial protection benefits
Medical insurance
Dental insurance
Vision insurance
Life insurance
Disability insurance
Flexible Time Off (FTO) for U.S.-based exempt employees
11 paid company holidays per year
160 hours of paid vacation annually for new hires for non-exempt employees, RayzeBio employees, and employees located in Puerto Rico
3 optional holidays
Paid sick leave, depending on eligibility
Up to 2 paid volunteer days per year
Summer hours flexibility
Medical, personal, parental, caregiver, bereavement, or military leaves of absence
Annual Global Shutdown between Christmas Day and New Year's Day