Director, Clinical Data Management – Radiopharma

Bristol Myers Squibb

United States

Remote

USD 210,000 - 263,000

Full time

14 days+

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Benefits offered by this job

Health Coverage

Wellbeing Support

Financial Well-being and Protection

Paid Time Off

Job summary

RayzeBio, a Bristol Myers Squibb company, seeks a Director of Clinical Data Management to lead end-to-end data management across a new product's clinical studies. You will drive strategy, ensure data quality, and collaborate with CROs and internal teams to enable decision-ready data from startup to submission.

The role requires 10+ years in pharma/biotech data management, oncology experience, and proven CRO oversight.

Qualifications

Bachelor’s or Master’s degree in Life Sciences, Computer Science, Mathematics, Health Sciences, or a related field.
Minimum of 10 years data management experience in pharmaceutical/biotech/CRO industry.
Demonstrated experience leading study teams, vendors, or direct/indirect reports.
In-depth Oncology experience is required.
Proven ability to manage CRO relationships and oversee data management deliverables.
Experience utilizing AI-enabled tools to improve productivity and efficiency.

Responsibilities

Serve as the Clinical Data Management program lead for a new product and lead the individual studies within that program, providing strategic and hands-on data management leadership from study start-up through database lock.
Develop and drive the data management strategy for the assigned new-product program, including study start-up planning, database build oversight, data review approach, risk management, database lock, and submission readiness.
Lead data management execution at both the program and study level in partnership with study teams, ensuring high-quality, timely, and decision-ready clinical trial data across all studies within the program.
Oversee CROs and data management vendors supporting the program and its studies, ensuring clear expectations, accountability, quality, compliance, and adherence to study and program timelines.
Partner cross-functionally with Biostatistics, Statistical Programming, Clinical Operations, Medical Monitoring, Safety, Regulatory Affairs, and other stakeholders to align on program priorities, data quality expectations, and deliverables.
Lead ongoing cross-functional data review activities and ensure timely identification, escalation, and resolution of data issues, trends, risks, and quality concerns.
Oversee or contribute to key data management documentation, including Data Management Plans, edit check specifications, validation plans, reconciliation plans, data transfer agreements, data review plans, and database lock documentation.
Willing to travel approximately 10% of the time. Evening and weekend work may be required.
Leverages AI to drive program, portfolio, or functional performance through prioritization and scaled adoption.