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Director, Clinical Data Management

Job in New York, New York County, New York, 10261, USA
Listing for: Syndax Pharmaceuticals
Full Time position
Listed on 2026-03-08
Job specializations:
  • IT/Tech
    Data Security, Data Analyst, Data Science Manager, Data Warehousing
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below
Location: New York

Syndax Pharmaceuticals is looking for a Director, Clinical Data Management

At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies.

The Role

This position is a strategic leader responsible for overseeing the design, implementation, and oversight of clinical data systems and processes across multiple clinical development programs. The Director directs a team in delivering high-quality clinical data in alignment with regulatory requirements, corporate goals, and operational efficiency. The role contributes to the long-term success of the function through data-driven strategies, innovation in systems and processes, and strong cross-functional partnerships.

The Director may also be responsible for projects that have been contracted with a service provider, as well as internal projects.

Key Responsibilities
  • Collaborate with senior leadership to define and implement functional and organizational strategy aligned with corporate objectives; participate in long-term planning and policy development.
  • Development and execution of data quality strategies, risk-based data review plans, and cross-study harmonization.
  • Direct the design, testing, validation, and maintenance of clinical databases and electronic data capture (EDC) systems.
  • Ensure consistent application of CDM standards, tools (e.g., CDISC, Medidata Rave), and procedures.
  • Oversee issue resolution and data integrity across outsourced vendors and internal teams>

    Provide proactive input into clinical protocol design to ensure data collection strategies align with scientific and regulatory requirements.
  • Review and contribute to clinical protocols and statistical analysis plans to ensure alignment with data collection objectives; cross-project consistency and standardization of case report forms.
  • Partner with internal stakeholders to align timelines and data delivery requirements.
  • Participate in cross-functional study teams; influence protocol design, study setup, and data strategy from study start to submission.
  • Actively support submission readiness, including data integration and final deliverables for regulatory filings.
  • Participate in protocol development, clinical study reports (CSR), and submission activities.
  • Manage relationships with CROs and third-party vendors, ensuring alignment with contractual deliverables and performance expectations.
  • Establish standards and oversight processes for EDC setup, CRF development, data validation, discrepancy management, and database lock.
  • Drive consistency and scalability through implementation of standards (e.g., CDISC/CDASH/SDTM) and SOPs.
  • Development and improvement of clinical data management processes and tools.
  • Lead and mentor Clinical Data Managers; provide coaching and foster a high-performing and collaborative environment.
  • Participate in the evaluation of organizational needs, defining resource strategies, and managing departmental budgets and headcount planning.
Desired Experience/Education and Personal Attributes
  • Bachelor’s degree in related scientific discipline; advanced degree preferred.
  • 12+ years of progressive experience in clinical data management with leadership responsibility at a sponsor organization.
  • Expert knowledge of clinical data management.
  • Deep expertise of industry standards including CDISC/CDASH, SDTM, ICH-GCP, 21 CFR Part 11, and regulatory submission requirements.
  • Proven success leading large-scale global studies, vendor oversight and working in both in-house and outsourced models.
  • Expertise knowledge and hands on experience with EDC systems (e.g., Medidata Rave, Veeva), clinical systems integration, and risk-based monitoring frameworks required.
  • Exceptional leadership, analytical, and communication skills with the ability to influence senior stakeholders and executives.
Location

Syndax’s corporate office is in New York, NY.

Compensation

Syndax offers a total compensation and rewards package that is among the most competitive in the industry. Base pay is just one element of our package and is determined within a range…

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