Director, Biostatistics

🕒 September 23

🇺🇸 United States – Remote

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 22%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Pulmovant

WebsiteLinkedInAll Job Openings

11 - 50 employees

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

Pulmovant is a company committed to transforming the lives of patients with pulmonary diseases by developing innovative therapies. Their lead product, mosliciguat, aims to provide a once-daily, inhaled treatment for pulmonary hypertension, distinguished by its novel sGC activation mechanism. With a singular focus on addressing the unique needs of patients suffering from pulmonary conditions, Pulmovant is engaged in extensive clinical trials to advance its pioneering treatment options.

📋 Description

• Serve as lead biostatistician for Pulmovant's Phase 3 PHrontier program, including protocol development, statistical analysis plans (SAPs), and sample size/power calculations • Partner with Clinical Development and Regulatory on trial design decisions, including endpoint selection and interim analysis strategy • Oversee CRO/vendor biostatistics deliverables, ensuring quality and timeline adherence • Lead statistical input for regulatory submissions, including NDA/BLA submissions and responses to health authority queries • Collaborate with Data Management on CRF design, database structure, and data quality standards • Present statistical results and methodology to internal leadership and external stakeholders, including DSMBs and advisory boards • Mentor junior biostatistics staff or contractors as the function scales • Contribute to departmental initiatives, standards, process improvements, talent development, resource planning, and inspection readiness

🎯 Requirements

• PhD or MS in Biostatistics, Statistics, or related field • 8+ years of biostatistics experience in clinical drug development, including direct Phase 3 experience • Deep expertise in SAS and/or R for clinical trial analysis • Strong understanding of ICH/FDA statistical guidance and GCP, ICH standards, and CDISC principles • Experience managing CRO biostatistics relationships • Excellent cross-functional communication skills, able to translate statistical findings for non-statistician stakeholders • Comfortable operating in a lean, scaling clinical-stage environment