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3 дня назад

Senior Statistical Project Leader (Director)

178 500 - 257 833$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior/director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Statistical Project Leader (Director) (Biostatistics/Oncology): Providing statistical leadership for clinical development studies and solid tumor projects with an accent on advanced statistical solutions, study design, and regulatory submissions. Focus on managing complex trial projects, representing statistics in regulatory meetings, and collaborating with cross-functional and senior leadership teams.

Location: Cambridge, MA; hybrid. US and Puerto Rico residents only.

Salary: $178,500–$257,833 per year

Company

hirify.global is an R&D-driven, AI-powered biopharma company developing medicines and vaccines through immunoscience, quantitative science, data, and digital platforms.

What you will do

  • Provide statistical leadership and clinical expertise for solid tumor clinical development planning and study design.
  • Contribute to clinical development plans, protocols, statistical analysis plans, clinical study reports, regulatory documents, and submissions.
  • Plan, monitor, and manage multiple complex clinical trial projects, including timelines, processes, resources, and operational standards.
  • Collaborate with project teams, statistics leaders, cross-functional partners, and senior leadership.
  • Represent statistics in regulatory meetings, scientific and technology working groups, and cross-functional initiatives.

Requirements

  • PhD in Statistics or a related discipline with at least 8 years of pharmaceutical clinical development experience, or MS with at least 10 years of experience.
  • Experience may include work with biotech, pharmaceutical companies, CROs, health authorities, or academic clinical research centers.
  • Strong understanding of clinical development and advanced statistical concepts and techniques.
  • Successful experience with clinical development activities, regulatory submissions, and interactions with regulatory agencies or external stakeholders.
  • Demonstrated leadership, communication, interpersonal, and project management skills.
  • Must be a US or Puerto Rico resident; the role is hybrid in Cambridge, Massachusetts.

Nice to have

  • Experience in oncology, especially solid tumors.
  • Published research findings, technical articles, or industry insights.
  • Experience representing an organization in consortia or professional associations.

Culture & Benefits

  • Supportive, future-focused environment with opportunities for promotion and lateral career development.
  • Health and wellbeing benefits, including healthcare, prevention, and wellness programs.
  • At least 14 weeks of gender-neutral parental leave.
  • Patient-informed drug development and work with AI, data, and digital platforms.
  • Inclusive workplace committed to equal opportunity and diverse perspectives.

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