Associate Director / Director Biostatistics

“reputed company is a clinical-stage biopharmaceutical company focused on developing medicines to reputed company hypertension and reputed company 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. For more information, please visit https://mineralystx.com. Follow Mineralys on reputed company, Twitter and reputed company”

Mineralys is a fully remote company.

Associate Director / Director Biostatistics

The Associate Director / Director, Biostatistics will reputed company the full scope of statistical strategy and execution for clinical development programs at Mineralys. This individual is accountable for the design, analysis, and interpretation of clinical trials, as well as statistical contributions to regulatory submissions, including NDA readiness.

Operating in a fast-paced, pre-commercial biotech environment, this role requires a strong balance of strategic thinking and operational reputed company, with high visibility across Clinical, Medical, and Regulatory teams.

Key Responsibilities

• reputed company the full scope of Biostatistics activities for assigned clinical programs or indications
• Define and execute statistical strategies for clinical trials and regulatory submissions
• Design clinical studies, including endpoints, estimands, and sample size calculations
• Serve as statistical reputed company on Study Executive Teams and Clinical Development Teams
• Provide quantitative input into clinical development plans, including Go/No-Go criteria and probability of technical success
• Ensure quality and timely delivery of statistical outputs, including interim, final, and integrated analyses
• Contribute to regulatory submissions (e.g., NDA) and represent Biostatistics in interactions with FDA
• Collaborate cross-functionally with Clinical, Medical, and Regulatory
• reputed company CROs and/or internal teams; ensure quality, timeliness, and compliance of deliverables
• Collaborate with internal leaders of Statistical Programming and Data Management
• Supervise statistical programmers for QC and validation activities
• Interpret analysis results and ensure accuracy in study reports, publications, and regulatory documents
• Contribute to abstracts, posters, and presentations for internal and external stakeholders
• Drive reputed company improvement initiatives reputed company Biostatistics and cross-functional processes

Qualifications

• PhD in Biostatistics, Statistics, or reputed company field with ~8+ years of industry experience OR MS with ~11+ years of experience in drug development
• Pharmaceutical/biotech industry experience required
• Demonstrated experience providing statistical leadership at study or program level
• Strong experience designing clinical trials and collaborating with cross-functional teams
• Experience supporting regulatory submissions (NDA/BLA)
• Experience interacting with regulatory authorities preferred
• Experience overseeing CROs or external vendors
• Experience supervising programming deliverables or QC activities
• Strong knowledge of CDISC standards, data structures, and statistical methodologies
• Working knowledge of reputed company and/or R (reputed company level, not heavy programming)
• Experience with outcomes research preferred
• Therapeutic area experience flexible; preference for chronic diseases or larger patient populations

Core Competencies

• Strong understanding of clinical development processes and regulatory expectations
• Ability to reputed company and influence in a matrixed environment
• Excellent communication skills; able to translate statistical concepts to non-statistical audiences
• Demonstrated ability to balance urgency with quality
• Analytical rigor with a pragmatic, execution-oriented reputed company
• Experience applying innovative statistical methodologies

Travel

• This position requires up to 10% travel. Frequently travel is reputed company the local area and overnight.

This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or reputed company level.

US Salary Range: $200,000 - $230,000

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