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Director Data Management information

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$54K

$154.9K

$244K

How much do director data management jobs pay per year?

As of Jun 8, 2026, the average yearly pay for director data management in the United States is $154,873.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,000.00 and $189,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Director of Data Management, and why are they important?

To thrive as a Director of Data Management, you need extensive experience in data governance, database architecture, and analytics, usually backed by a relevant degree and progressive leadership roles. Familiarity with enterprise data management tools (such as Informatica or Collibra), advanced SQL, and data privacy regulations is crucial, and certifications like CDMP can be advantageous. Strong leadership, strategic thinking, and effective communication enable you to guide teams and align data initiatives with business objectives. These competencies ensure data integrity, compliance, and the delivery of valuable insights that drive organizational success.

What Does a Director of Data Management Do?

As a director of data management, your responsibilities include all operational and strategic aspects of data management, especially regarding product development and decision-making. You monitor a team and handle data management to develop, implement, and complete projects while ensuring a high level of data quality based on regulatory standards. You also manage resources and the budget, lead the development of Product Lifecycle Management (PLM) roadmaps, and develop dashboards and metrics to show the status of data governance and quality. You are also expected to oversee the collection of information into the business data warehouse, build analytic solutions using various big data techniques and tools, and document these solutions and the technical data architecture. Other duties include providing guidance using best industry practices, working with many client databases, and interpreting flag codes.

What are some common challenges faced by a Director of Data Management when implementing data governance frameworks?

A Director of Data Management often encounters challenges such as securing buy-in from stakeholders across various departments, integrating disparate data sources, and ensuring consistent data quality and compliance with regulatory requirements. Balancing the need for robust security with accessibility for business users can also be complex. Addressing these challenges requires strong communication skills, a clear data strategy, and effective collaboration with IT, legal, and business teams.

What is the difference between Director Data Management vs Data Analyst?

AspectDirector Data ManagementData Analyst
Required CredentialsBachelor's or Master's in Data Science, IT, or related field; often with leadership experienceBachelor's in Statistics, Data Science, or related field; often entry to mid-level experience
Work EnvironmentStrategic leadership, overseeing data teams, managing data governanceData collection, analysis, reporting, supporting decision-making
Employer & Industry UsageUsed in large corporations, tech, finance, healthcareCommon across industries for data-driven roles

The main difference is that a Director Data Management focuses on strategic oversight, data governance, and leading data teams, while a Data Analyst primarily handles data analysis, reporting, and supporting business decisions. The Director role involves higher-level management and planning, whereas Data Analysts execute specific data tasks.

What is a Director of Data Management?

A Director of Data Management is a senior leader responsible for overseeing an organization's data strategy, governance, and operations. They ensure that data is collected, stored, and used efficiently and securely to support business objectives. This role often involves managing a team, setting data policies, ensuring compliance with regulations, and working with other departments to leverage data for decision-making and innovation.
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Associate Director / Director, Data Management

Associate Director / Director, Data Management

Beam Therapeutics

Cambridge, MA

Other

Posted 16 days ago


Job description

Position Overview:

Reporting to the Senior Director, Clinical Data Management, the Associate Director / Director, Clinical Data Management will serve as the dedicated data management lead for our Liver franchise. Initially supporting a single study within the program, this individual will grow with the franchise as it expands to include additional studies within the same program and, ultimately, other programs across the franchise portfolio.

This role offers a unique blend of hands-on study oversight and strategic leadership, making it an ideal opportunity for a candidate who thrives at the intersection of execution and innovation, in a fastpaced biotech environment where clarity, quality, and collaboration are critical.

This is a highly visible role working crossfunctionally with Clinical Development, Biostatistics, Statistical Programming, Regulatory, Quality, and external partners to ensure data integrity, inspection readiness, and timely delivery of data supporting key development and regulatory milestones.

Primary Responsibilities:

Program & Study Ownership

  • Lead sponsor side clinical data management activities across multiple concurrent studies within a defined therapeutic area.
  • Own data management execution from study start-up through database lock and archival for concurrent studies, including late stage and registrational trials.
  • Ensure data quality, integrity, and traceability to support interim analyses, CSRs, DSURs, IB updates, and program specific regulatory interactions.
  • Proactively identify data risks, trends, and operational dependencies; communicate issues early with clear, solution-oriented recommendations.

CRO & Vendor Oversight

  • Serve as the primary data management contact for CROs and third-party data vendors.
  • Oversee outsourced CDM activities to ensure timely, high-quality deliverables aligned with sponsor' expectations.
  • Monitor CRO and vendor performance, escalating risks and proposing mitigation strategies in partnership with the Senior Director of Data Management.

Data Standards, Systems & Process Contribution

  • Contribute expert input to the development and evolution of data management standards, processes, tools/systems and vendor operating models as the organization scales its clinical portfolio.
  • Provide hands-on leadership for:
    • CRF design and cross functional review
    • Edit check specifications and user acceptance testing
    • Data Management Plans and CRF Completion Guidelines
    • External data transfer specifications
  • Apply CDASH/CDISC expertise and partner with Statistical Programming to support SDTM readiness, validation outputs, Reviewer's Guides, and define.xml.

Inspection Readiness

  • Support inspection readiness activities across assigned programs, ensuring documentation and data traceability meet regulatory expectations.
  • Serve as a key data management participant during audits and inspections, in coordination with the Senior Director and Quality.
  • Ensure data management deliverables remain inspection ready throughout the study lifecycle.

Cross-Functional Partnership

  • Collaborate closely with Clinical Operations, Biostatistics, Statistical Programming, Medical Monitoring, Regulatory, and Quality.
  • Communicate complex data issues clearly and effectively to stakeholders with varying technical backgrounds.
  • Build trust as a pragmatic, detail-oriented partner who balances scientific rigor with efficient execution.

Required Qualifications:

  • BS or MS degree in a scientific or health-related field.
  • 10+ years of experience in clinical data management within pharmaceutical/biotech and/or CRO environments.
  • Demonstrated sponsor-side ownership of Phase I, II and III studies, from start-up through closure for multiple clinical studies.
  • Strong hands-on experience with EDC systems (e.g., Medidata RAVE, Veeva EDC, Oracle Inform).
  • Deep knowledge of CDASH/CDISC, GCP/ICH, and FDA regulatory expectations.
  • Proven experience overseeing CROs and external data vendors.
  • Experience developing reports using J-Review and/or other CDM reporting tools.
  • Prior IND, as well as NDA/BLA (filing/submission) experience, is highly desirable.
  • Must be self-motivating, with strong analytical, organizational, and communication skills, with the ability to manage complexity across multiple studies.
  • Demonstrated ability to navigate evolving priorities and drive timelines forward with focus and composure in a fast-moving organization.

Preferred Qualifications:

  • Experience and knowledge of gene/cell therapy and/or rare disease.
  • Prior experience supporting registrational or pre registrational programs.