Director, Biostatistics

Benefits

Parental leave

Not verified

Non-birth-parent leave

Not verified

Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

Not verified

Relocation assistance

Not verified

Childcare support

Not verified

Learning budget

Not verified

Verification

Not verified

Salary

Not verified not verified - source not recorded; timestamp not recorded

401(k) match

Not verified

Was this benefit information wrong? Tell us.

Schedule

Shift type

Not verified

Weekend work

Not verified

Application

Cover letter

Not verified

Assessment

Not verified

Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Director, Biostatistics South San Francisco, CA The Position As the Director, Biostatistics, you will play an important role in shaping and supporting the clinical development of Maze's therapeutic programs. You will partner closely with Clinical Science, Regulatory Affairs, Clinical Pharmacology, Development Science, and Translational Science to ensure our clinical studies are robust, data-driven, and impactful. In this role, you'll oversee biostatistical strategy and execution, from study design through regulatory submissions, balancing hands-on expertise with strategic leadership. You will also represent Biostatistics on clinical study teams, guide interpretation of complex data, and oversee CRO partners to ensure high-quality statistical deliverables. The position will report to the Vice President, Biometrics. The Impact You'll Have - Serve as the biostatistics lead for clinical studies, providing expert input on study design, endpoints, and statistical strategy - Oversee and contribute to completion of all technical and operational statistical activities for a group of clinical trials. Ensure development and review of statistical analysis plans (SAPs), including complex and innovative methodologies - Collaborate with cross-functional partners in protocol development, study design discussions, and data interpretation - Partner with Statistical Programming to generate and validate analyses for internal use, publications, and regulatory submissions - Oversee CRO execution of statistical tasks: managing timelines, quality, and analytical approaches - Represent biostatistics in regulatory interactions (FDA, EMA, PMDA, etc.), contributing to briefing documents, meeting preparation, and responses to agency questions - Contribute to clinical study reports (CSRs), integrated summaries (ISS/ISE), and regulatory submissions (NDA/BLA/MAA) - Apply advanced statistical techniques to explore,

Read the full description at www.mazetx.com. FewerJobs shows a source-linked preview and links to the original posting.