Director, Statistical Programming

Mineralys Therapeutics

1d•$235,000 - $248,000•Remote

About The Position

Mineralys Therapeutics is a clinical-stage biopharmaceutical company focused on developing medicines to target hypertension and related comorbidities such as chronic kidney disease (CKD), obstructive sleep apnea (OSA) and other diseases driven by dysregulated aldosterone. Its initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor. Mineralys is headquartered in Radnor, Pennsylvania. Mineralys is a fully remote company. The Director Statistical Programmer (SP) reports to the SVP, Biometrics and is accountable for the production of SDTM and ADAM datasets and Tables, Listings, and Graph output (TFLs) for clinical studies. They will collaborate with partner functions in the Clinical Development Department (e.g. Clinical Operations, Clinical Research, Biostatisticians). They will be accountable for Medical Affairs support by providing output for posters, presentations, and publications.

Requirements

BS/BA degree and 10+ years of experience in analyzing clinical data OR MS in statistics or related area and 7+ years of experience in analyzing clinical data.
Experience with FDA submissions and the provision of data submission packages
Experience in multiple areas outside of clinical development (e.g. pre-clinical, medical affairs, RWE)
Deep knowledge of the SAS programming language
Demonstrated accomplishments in automatization (usually through SAS macro development)
Working knowledge of at least one other programming language, preferably R
Experience with using genAI to create programming code or data processing algorithms.
Ability to work in an interdisciplinary team in a collaborative way
Represents biometrics in a positive and professional manner
Ability to work in a fast-paced team environment with fluctuating priorities
Common sense and solution-oriented mindset
Intellectual curiosity with a sense of pragmatic implementation of new ideas
Ability to communicate effectively in English, both orally and in writing.
Strong understanding of clinical development processes and regulatory expectations
Ability to lead and influence in a matrixed environment
Demonstrated ability to balance urgency with quality
Analytical rigor with a pragmatic, execution-oriented mindset

Responsibilities

Accountable for all core SP deliverables (SDTM, ADAM, TFLs)
May also be accountable for clinical programming tasks (creation of SDTM and complex edit checks)
Provides ongoing data review by providing programmed edit checks, risk-based monitoring metrics, and draft TFLs
With IT, defines our programming environment and its validation
Responsible for the development of standards, SOPs, and best practices
The role is a combination of vendor oversight, supervision of more junior statistical programmers, and some hands-on work.
The Director SP will supervise assigned junior programmers, both contractors and regular staff members.