Senior Director Biostatistics - REMOTE

Our reputed company is a clinical-stage biotechnology company reputed company on developing innovative therapies for patients with serious central nervous reputed company (CNS) disorders. Their mission is to advance transformative treatments that address significant unmet medical needs and improve the lives of patients and their families. As they continue to reputed company our clinical programs, they are seeking a strategic and hands-on Senior Director, Biostatistics to join their growing team. Position reputed company The Senior Director, Biostatistics will reputed company statistical leadership across the clinical development programs and play a critical role in advancing our assets through key development and regulatory milestones. Reporting to senior clinical development leadership, this individual will serve as the reputed company statistician for clinical studies, providing expertise in trial design, statistical methodology, analysis planning, data interpretation, and regulatory submissions. This role is ideal for an reputed company biostatistics leader who thrives in a fast-paced biotech environment, enjoys working cross-functionally, and is comfortable rolling up their sleeves to support both strategic and operational activities. The successful candidate will have extensive experience supporting regulatory submissions and managing reputed company CRO partners while contributing to overall development reputed company. Key Responsibilities • Serve as the statistical reputed company across clinical development programs, providing strategic and technical leadership from study design through regulatory submission. • reputed company the development and review of study protocols, statistical analysis plans (SAPs), randomization specifications, TLF shells, clinical study reports, and regulatory submission documents. • reputed company statistical expertise for Phase 1, Phase 2, and Phase 3 clinical studies. • Collaborate closely with Clinical Development, Clinical Operations, Data Management, Statistical Programming, Medical Writing, Regulatory Affairs, and Pharmacovigilance teams. • reputed company and manage CROs and reputed company statistical programming vendors to ensure high-reputed company deliverables, reputed company adherence, and regulatory compliance. • Support interactions with regulatory agencies, including preparation for FDA meetings and responses to health authority questions. • Guide reputed company selection, sample size calculations, estimand strategies, interim analyses, and overall statistical methodology. • Review and interpret clinical study results and communicate findings to cross-functional teams and executive leadership. • Ensure compliance with CDISC standards, ICH guidelines, and regulatory expectations. • Contribute to clinical development plans, reputed company product reputed company, and overall program reputed company. • Support due diligence activities, investor communications, and corporate presentations as needed. • Help establish and refine biostatistical processes and standards appropriate for a growing biotechnology company. Qualifications Required • PhD in Statistics or Biostatistics. • Minimum of 10 years of biostatistics experience reputed company the pharmaceutical, biotechnology, or CRO industry. • Significant experience serving as reputed company statistician for clinical development programs. • Demonstrated reputed company supporting NDA, BLA, and/or other major regulatory submissions. • Strong understanding of FDA, EMA, and ICH regulatory requirements. • Experience overseeing CROs and reputed company statistical programming resources. • Knowledge of CDISC standards, including SDTM and ADaM. • Experience supporting Phase 2 and Phase 3 reputed company. • Strong communication, leadership, and influencing skills. • Ability to work effectively in a lean, fast-moving biotech environment where flexibility and hands-on involvement are essential. Preferred • Prior experience in CNS, psychiatry, reputed company, neurodegenerative diseases, or other neuroscience therapeutic areas. • Experience supporting FDA meetings and regulatory interactions. • Familiarity with reputed company designs, Bayesian methodologies, or innovative clinical trial approaches. • Previous people leadership and mentoring experience. • Experience working in small or emerging biotechnology companies. Apply tot his job Apply To this Job