Associate Director, Clinical Data Management

Bristol Myers Squibb

Associate Director leading clinical data management for RayzeBio, a Bristol Myers Squibb oncology biotech. Overseeing CROs, vendors, data quality, and radiopharmaceutical clinical trials.

Posted 8/5/2026full-timeRemote • 🇺🇸 United StatesSenior💰 $173,217 - $209,899 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in data management within the pharmaceutical and biotech industries, with a strong focus on regulatory compliance, CRO management, and the use of EDC systems. Proven ability to lead clinical data management efforts and enhance team performance through analytical insights and effective communication.

Highest-signal resume keywords

Clinical Data ManagementEDC Systems (Medidata RAVE, Veeva)GCP, CDISC/CDASH, ICH GuidelinesCRO Relationship ManagementOncology Therapeutic Area Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data ManagementTrend AnalysisRegulatory ComplianceQuality ReportingData Visualization

Soft Skills

Verbal CommunicationWritten CommunicationAnalytical SkillsProblem-Solving

Tools & Technologies

EDCIVRSCTMSETMFClinical Project Management Tools

Industry Keywords

PharmaceuticalBiotechCROClinical TrialsLife Science

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Provide data management leadership, insight, and support to internal and external projects and clinical trials
Serve as lead Clinical Data Manager for multiple clinical trials when needed
Ensure collected data meets study objectives and company quality standards
Manage and oversee data management personnel and CRO/vendor activities
Ensure CRO adherence to project timelines from study startup through closeout
Participate in cross-functional meetings and provide project status, issue, and milestone updates
Review data using listings and visualization tools for performance and quality reporting
Conduct within-study and cross-study trend analyses
Lead third-party vendor interactions regarding collection, transmittal, and transfer of study-specific data
Contribute to SOP development and updates for regulatory compliance and operational needs
Travel approximately 10%

Requirements

What you’ll need

Bachelor’s degree required
Minimum of 6 years of data management experience in the pharmaceutical, biotech, or CRO industry
Extensive hands-on experience in all aspects of data management
Bachelor’s degree in Life Science, mathematics, or health-related fields preferred
Experience in the Oncology therapeutic area preferred
Proven ability to manage CRO relationships and oversee data management deliverables
Strong knowledge and experience with EDC systems, including Medidata RAVE or Veeva
Solid knowledge of GCP, CDISC/CDASH data structures, ICH guidelines, and FDA regulations
Excellent verbal and written communication skills
Strong analytical and problem-solving abilities
Ability to apply AI to improve team execution and decision-making
Proficiency in clinical systems including EDC, IVRS, CTMS, eTMF, and other clinical project management tools
Ability to learn new systems as needed
Approximately 10% travel required

Benefits

Comp & perks

Additional incentive cash and stock opportunities (based on eligibility)
Medical, pharmacy, dental, and vision care
BMS Well-Being Account
BMS Living Life Better
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
Survivor support
Flexible time off for US exempt employees, with manager approval
11 paid national holidays
160 hours annual paid vacation for eligible new hires, with manager approval
3 optional holidays
Unlimited paid sick time, based on eligibility
Up to 2 paid volunteer days per year
Summer hours flexibility, based on eligibility
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
Annual Global Shutdown between Christmas and New Years Day, based on eligibility