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Posted May 3, 2026

Director, IT - Governance, Risk & Compliance

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DIRECTOR, IT GOVERNANCE, RISK & COMPLIANCE



COMPANY OVERVIEW:

 

Zentalis® Pharmaceuticals, Inc. is a clinical-stage biopharmaceutical company developing azenosertib (ZN-c3), a potentially first-in-class and best-in-class WEE1 inhibitor for patients with Cyclin E1+ platinum-resistant ovarian cancer (PROC). Azenosertib is being evaluated as a monotherapy and in combination across multiple tumor types in clinical trials and has broad franchise potential. In clinical trials, azenosertib has been well tolerated and has demonstrated anti-tumor activity as a single agent across multiple tumor types. The Company is also leveraging its extensive experience and capabilities to translate its science to advance research on additional areas of opportunity for azenosertib outside PROC.

 

POSITION SUMMARY:


The Director of IT Governance, Risk & Compliance (IT GRC) is a senior leader responsible for maturing the company's IT governance framework, risk management program, and regulatory compliance posture. This role owns the IT GRC function serving as the primary liaison between Information Technology, Quality Assurance, Legal, Finance, and external auditors to ensure that IT systems, processes, and controls meet all applicable regulatory and industry standards. Operating within a highly regulated biotech environment, this leader will drive compliance with FDA 21 CFR Part 11, GxP system validation, SOX IT General Controls (ITGCs), HIPAA, NIS2 Directive, and cybersecurity frameworks (NIST, ISO 27001). Reporting directly to the VP of IT the Director is a key member of the IT leadership team with accountability for enterprise-wide IT risk strategy, audit outcomes, and regulatory readiness. This role carries significant cross-functional influence and is expected to shape company culture around governance and compliance.

 

ESSENTIAL DUTIES AND RESPONSIBILITIES:


IT Governance


Risk Management


Regulatory Compliance & Audit


Policy, Training & Awareness

Advise IT project teams and technology owners on control requirements during system design and implementation


KNOWLEDGE/SKILLS/ABILITIES REQUIRED:


Required

Bachelor's degree in Information Technology, Computer Science, Life Sciences, or a related field; Master's degree strongly preferred.

12+ years of progressive IT GRC, IT audit, or IT compliance experience, with at least 5 years in a biotech, pharmaceutical, or medical device environment.

Minimum 4 years of people management experience, including managing managers or senior individual contributors.

Deep expertise in FDA 21 CFR Part 11, GxP computer system validation (CSV), and SOX IT General Controls.

Proven track record managing IT audit processes and working directly with external auditors (Big 4 preferred) and regulatory agencies.

Strong knowledge of IT risk management frameworks (NIST CSF, ISO 27001/27002, COBIT) and demonstrated ability to set and execute multi-year GRC strategy.

 

Preferred

Master's degree in Information Systems, Business Administration, or a related discipline.

Professional certifications: CISA, CRISC, CGEIT, CISSP, or CIPP.

Experience with cloud GRC platforms (ServiceNow GRC, Archer, Vanta, Drata) and validated cloud environments (AWS, Azure, GCP).

Familiarity with HIPAA/HITECH, NIS2 Directive, GDPR, and CCPA compliance in a clinical or research setting.

Prior experience supporting IND/NDA/BLA submissions or FDA facility inspections.

Experience standing up a GRC function or program from an early-stage maturity baseline.

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