Director, Clinical Data Management

Bristol Myers Squibb

Clinical data management director leading oncology trial data strategy and execution for RayzeBio, a Bristol Myers Squibb radiopharmaceutical biotech. Driving CRO oversight, data quality, database lock, and submission readiness.

Posted 8/5/2026full-timeRemote • California • 🇺🇸 United StatesLead💰 $200,980 - $243,544 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in Clinical Data Management, leading cross-functional teams and managing CRO relationships to ensure high-quality clinical trial data. Proficient in utilizing AI-enabled tools and EDC systems to enhance productivity and compliance within the Oncology therapeutic area.

Highest-signal resume keywords

Clinical Data ManagementOncology Therapeutic AreaEDC Systems (Medidata RAVE, Veeva)GCP, CDISC/CDASH, ICH GuidelinesCRO Relationship Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data Management StrategyDatabase Build OversightData ReviewRisk ManagementDatabase LockSubmission ReadinessData Management PlansValidation PlansData Transfer AgreementsAI-Enabled Tools

Soft Skills

LeadershipMentoringCommunicationAnalytical SkillsProblem-Solving

Industry Keywords

PharmaceuticalBiotechCROClinical TrialsRadiopharmaceutical

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serve as the Clinical Data Management program lead for a new product and lead individual studies from study start-up through database lock
Develop and drive data management strategy, including study start-up planning, database build oversight, data review, risk management, database lock, and submission readiness
Lead program- and study-level data management execution to deliver high-quality, timely, decision-ready clinical trial data
Oversee CROs and data management vendors, ensuring accountability, quality, compliance, and adherence to timelines
Partner with Biostatistics, Statistical Programming, Clinical Operations, Medical Monitoring, Safety, Regulatory Affairs, and other stakeholders
Lead cross-functional data reviews and identify, escalate, and resolve data issues, trends, risks, and quality concerns
Oversee or contribute to Data Management Plans, edit check specifications, validation plans, reconciliation plans, data transfer agreements, data review plans, and database lock documentation
Leverage AI to drive program, portfolio, or functional performance through prioritization and scaled adoption
Travel approximately 10% of the time; evening and weekend work may be required

Requirements

What you’ll need

Bachelor’s or Master’s degree in Life Sciences, Computer Science, Mathematics, Health Sciences, or a related field required
Minimum of 10 years of data management experience in the pharmaceutical, biotech, or CRO industry
Demonstrated experience leading study teams, vendors, or direct/indirect reports
Ability to guide, mentor, and develop others as applicable
In-depth experience in the Oncology therapeutic area required
Proven ability to manage CRO relationships and oversee data management deliverables
Experience utilizing AI-enabled tools to improve productivity and work efficiency
Strong knowledge and experience of 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
Radiopharmaceutical experience preferred

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 insurance
Life insurance
Accident insurance
Supplemental health insurance
Business travel protection
Personal liability protection
Identity theft benefit
Legal support
Survivor support
Flexible time off for eligible US exempt employees, with manager approval
11 paid national holidays
160 hours annual paid vacation for eligible RayzeBio exempt, non-exempt, and hourly employees, with manager approval
3 optional holidays
Unlimited paid sick time (eligibility-based)
Up to 2 paid volunteer days per year
Summer hours flexibility (eligibility-based)
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
Annual Global Shutdown between Christmas and New Years Day
Reasonable workplace accommodations/adjustments and ongoing support