Senior Manager, Statistical Programming & Analysis

Mirum Pharmaceuticals • Foster City, CA

8h • $190,000 - $210,000 • Hybrid

About The Position

Reporting directly to the Director, Statistical Programming & Analysis, the Senior Manager, Statistical Programming & Analysis will be responsible for the management and oversight of programming activities in support of the brelovitug program. The role will be responsible for providing operational oversight of statistical programming vendors as well as performing in-house programming activities in support of clinical trial analysis and reporting, regulatory filings, and internal decision-making processes.

Requirements

• Master’s degree in statistics, biostatistics, data science, or a closely related field preferred.
• 5+ years of experience as a statistical programmer within the biotech/pharmaceutical industry with at least 2 years of demonstrated study lead programming experience and career progression.
• Experience in effectively managing statistical programming vendors and/or internal statistical programming resources for the purposes of clinical trial reporting, regulatory filings, and key internal deliverables.
• Advanced SAS programming skills in performing clinical trial data analysis and reporting.
• Strong analytical skills and demonstrated experience in gathering, interpreting, and analyzing data in clinical research and drug development.
• Working knowledge of FDA and ICH GCP guidelines to ensure the appropriate conduct of clinical studies.
• Strong communication skills, ability to development rapport among cross-functional stakeholders, and passion to analyze complex issues to develop relevant and realistic programming solutions.
• Ability to at times take initiative to work with minimal supervision and efficiently adjust workload based upon changing priorities.

Nice To Haves

• Experience in regulatory GCP inspections/audits is a plus.

Responsibilities

• Provide programming expertise in support of statistical analysis across multiple clinical trials for inclusion in clinical study reports, regulatory submissions, periodic reporting, and publications.
• Perform oversight of statistical programming vendors to ensure quality and on-time delivery of programming packages.
• Develop and maintain CDISC-compliant and submission-ready SAS programs, SDTM, ADaM and summary tables and figures.
• Work collaboratively with multiple stakeholders to manage priorities and resources; understand and perform in accordance with regulatory standards and drug development principles.
• Monitor and evaluate ongoing clinical trial data and contribute to the resolution of data discrepancies.
• Contribute to overall Biometrics group in developing innovative processes to ensure high data quality and efficient reporting of analysis results.
• Ensure proper filing of study documentation consistent with regulatory compliance and conducive to inspection readiness.
• Take on initiative to stay current on relevant technologies, industry standards and guidelines to improve programming efficiency and facilitate review of clinical trial data.
• Other duties as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level