
Biotechnology • Pharmaceuticals
Amylyx Pharmaceuticals is a company dedicated to discovering and developing innovative treatments for diseases with high unmet needs. They focus on conditions such as Amyotrophic Lateral Sclerosis (ALS), Post-Bariatric Hypoglycemia (PBH), Wolfram Syndrome, and Progressive Supranuclear Palsy (PSP). Amylyx is committed to supporting patients and their loved ones, creating more moments of significance for them. They have recently acquired a Phase 3-ready GLP-1 receptor antagonist with FDA Breakthrough Therapy Designation and have shown positive results in clinical trials for Wolfram syndrome. The company emphasizes transparency, setting realistic expectations, and collaborating to make impactful changes in the treatment of neurodegenerative diseases.
201 - 500 employees
Founded 2020
🧬 Biotechnology
đź’Š Pharmaceuticals
November 18

Biotechnology • Pharmaceuticals
Amylyx Pharmaceuticals is a company dedicated to discovering and developing innovative treatments for diseases with high unmet needs. They focus on conditions such as Amyotrophic Lateral Sclerosis (ALS), Post-Bariatric Hypoglycemia (PBH), Wolfram Syndrome, and Progressive Supranuclear Palsy (PSP). Amylyx is committed to supporting patients and their loved ones, creating more moments of significance for them. They have recently acquired a Phase 3-ready GLP-1 receptor antagonist with FDA Breakthrough Therapy Designation and have shown positive results in clinical trials for Wolfram syndrome. The company emphasizes transparency, setting realistic expectations, and collaborating to make impactful changes in the treatment of neurodegenerative diseases.
201 - 500 employees
Founded 2020
🧬 Biotechnology
đź’Š Pharmaceuticals
• Provide a strategic leadership role in the Biometrics Team and cross-departmental program team to ensure the biometrics scopes and timelines defined to meet the corporate objectives • Lead and manage the biostatistics team and provide statistical strategies to drug development including development plans, innovative or adaptive study designs, and cross-study analyses including basic and complex statistical methodology implementation, data interpretations, regulatory submissions • Act at the lead presenter of statistical data and results of clinical trials to senior management, regulatory agencies, or individual investigators • Oversee execution of statistical tasks, resources, timelines and budgets for the function • Provide guidance and support to develop individual protocols and data analysis plans and determine appropriate statistical methodologies for analysis; analyze data and interpret results from clinical trials to meet objectives of the study protocol • Mentor biostatisticians and oversee execution of major statistics deliverables and milestones in collaboration with other functions • Build and maintain a partnership with CROs or individual consultants as needed, provide statistical oversight to tasks outsourced and assure adequate quality and consistency with company and industry standards • Participate and collaborate in database design meetings as needed to ensure high quality data evaluated and analysis requirements satisfied • Review and approve responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators • Review and ensure the accuracy of Statistical Review Aids submitted to regulatory agencies • Ensure compliance with GCP and other regulatory requirements
• PhD or equivalent advanced degree in statistics/biostatistics with 12+ years relevant work experience within pharmaceutical or biotechnology industry • Exemplary leadership, strategic thinking, and technical expertise in statistical analysis, with a proven track record of leading a high performing biometrics team • Expert knowledge of statistical methodologies such as longitudinal data analysis, Bayesian modeling and adaptive designs • Working knowledge of statistical and data processing software e.g., SAS and/or R • Good understanding of worldwide regulatory requirements and clinical trial expertise from early phase to late phase. NDA/MAA submission experience is desired • Strong oral and written communication skills. Ability to function effectively in a team and cross-functional environment • Advanced knowledge of the pharmaceutical industry, and overall drug development process • Strong project management skills. An understanding of biology of disease and drug discovery.
• Health insurance • 401(k) matching
Apply NowNovember 18
Assistant VP/Regional Asset Manager focusing on asset management strategies for affordable housing properties. Overseeing compliance, financials, and property performance across a regional portfolio.
November 18
10,000+ employees
Divisional Vice President leading regional directors at Five Below to ensure flawless execution and drive sales growth. Focus on customer satisfaction, team empowerment, and operational efficiency.
🇺🇸 United States – Remote
đź’° $194M Private Equity Round on 2010-10
⏰ Full Time
đź”´ Lead
đź‘” Vice President
🦅 H1B Visa Sponsor
November 18
Vice President of Investor Relations at TTM Technologies, focusing on investor relationships and communications. Engaging with stakeholders to convey TTM's strategic direction and financial performance.
November 18
501 - 1000
Regional Vice President managing partner programs focusing on client transitions and relationship management. Working with custodial partners and financial consultants to enhance services offered to clients.
🇺🇸 United States – Remote
đź’° $736.3k Funding Round on 2022-02
⏰ Full Time
đź”´ Lead
đź‘” Vice President
November 18
Vice President of Development leading real estate strategy and infrastructure development at NTT DATA. Responsible for executing regional development strategy aligned with corporate priorities and customer demand.
🇺🇸 United States – Remote
đź’µ $221k - $315.8k / year
⏰ Full Time
đź”´ Lead
đź‘” Vice President