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Amylyx

Director, Biostatistics

RemoteUnited States only· except United States, AK, Azerbaijan +3 more
Published
Role
Data Science
Experience
Lead
Employment
Full-time
Company size
Startup
$221k–$249k/yr
Check eligibility

Open to US only · except US, AK, AZ, HI, MI, TN. Set where you work from to check your eligibility.

No BS summary

Director of Biostatistics with PhD and 10+ years of experience in clinical trials, or MSc with 14+ years. Must have proficiency in SAS or R, CDISC standards, and clinical trial design (Phases I-III). Requires experience with ISS/ISE and strong communication/negotiation skills. Remote within the US, with travel to Cambridge, MA.

Core skills

BiostatisticsClinical Trial Design

Required skills

SASRCDISC standards

Optional skills

interactions with regulatory and health authorities

Required languages

English

What you'll do

  • Provide strategic leadership of statistical approaches on an assigned therapeutic area or a program, shaping clinical development plans from early design through regulatory submission and post-submission activities.
  • Serve as a statistical lead and thought partner to cross-functional teams and external stakeholders.
  • Lead the design and oversight of robust, innovative clinical trial designs that maximize probability of clinical and regulatory success, balancing scientific rigor with operational feasibility, while anticipating and proactively addressing potential regulatory challenges.
  • Oversee and/or contribute to key statistical deliverables, including protocols, statistical analysis plans, table/listing/figure shells, clinical study reports, integrated summaries of safety and efficacy, briefing documents, regulatory responses, and submission materials.
  • Oversee CRO and vendor statistical and programming activities to ensure quality, consistency, timeliness, and alignment with regulatory standards and company expectations.
  • Mentor, coach, and develop statisticians at varying levels of experience by providing technical guidance, fostering professional growth, and instilling best practices in statistical methods, data integrity, and regulatory compliance.
  • Synthesize and present statistical insights by preparing data packages and cross-functional presentations, effectively communicating strategies, assumptions, and implications to leadership, regulatory bodies, and scientific audiences.
  • Partner closely across functions to ensure alignment, collaboration, and timely execution of statistical deliverables that enable high-quality program success.
  • Engage in occasional travel to Cambridge, MA and other locations for collaboration and conferences, typically at least three times annually.

What they require

  • PhD in Statistics/Biostatistics, Mathematics, or related quantitative fields with a minimum of 10 years, or MSc with a minimum of 14 years of experience with clinical trials including late-phase studies.
  • Proficiency in scientific computing/programming (SAS or R) and hands-on implementation of advanced statistical analyses and simulations, deep knowledge of CDISC standards.
  • Proficiency in the design of clinical trials Phases I – III, in applying knowledge of general and cutting edge statistical / clinical trials methodologies to solve complex statistical problems in the clinical development programs and to ensure alignment with regulatory agencies and industry standards.
  • Demonstrate skills in the analysis and reporting of clinical trials; experience with integrated summaries of safety and efficacy (ISS and ISE).
  • Prior experience in interactions with regulatory and health authorities considered a plus.
  • Excellent written, verbal, and interpersonal communication skills, and strong negotiation, and organizational skills; must be able to work independently.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

Benefits

  • health insurance coverage
  • state tax regulations

Amylyx is a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).

🇬🇧 United KingdomBiotechStartupamylyx.com/
$221k–$249k/yr