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5 дней назад

Associate Director, Statistics (Biostatistics)

141 500 - 268 500$
Формат работы
onsite
Тип работы
fulltime
Грейд
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
Associate Director, Statistics (Biostatistics): Developing statistical strategies, protocols, and analyses for clinical research, real-world evidence studies, and health technology assessment submissions with an accent on biostatistical methodology, observational data, and regulated pharmaceutical research. Focus on designing evidence-generation programs, solving data and analytical issues, and leading cross-functional statistical work for drug development and life-cycle management.

Location: Florham Park, New Jersey, United States

Salary: $141,500–$268,500 annual base pay

Company

hirify.global develops medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

  • Provide statistical expertise for drug development, life-cycle management, medical affairs strategies, and scientific research programs.
  • Develop scientifically sound protocols and statistical analysis plans aligned with product strategy and regulatory requirements.
  • Design and analyze clinical, real-world evidence, and health technology assessment studies using clinical and real-world databases.
  • Introduce innovative statistical methodologies, evaluate analysis strategies, and address technical or data-related issues.
  • Lead cross-functional collaboration with Medical Affairs, Clinical Statistics, Data Sciences, Statistical Programming, vendors, regulatory agencies, and key opinion leaders.
  • Support health technology assessment submissions and ensure accurate, high-quality statistical reporting and publications.

Requirements

  • MS in Statistics, Biostatistics, or a related field with at least 10 years of experience, or PhD with at least 6 years of experience.
  • Expertise in experimental and real-world evidence study design, descriptive and inferential statistics, statistical modeling, and statistical programming.
  • Knowledge of confounding control and bias minimization in observational studies.
  • Strong leadership skills, including experience managing a programming group and cross-cultural or overseas teams.
  • Pharmaceutical or related industry experience, including drug development and life-cycle management in a regulated environment.
  • Strong written and oral communication skills, with the ability to explain statistical concepts to non-statisticians.

Culture & Benefits

  • Cross-functional, product-oriented collaboration focused on patient-centric evidence and healthcare decisions.
  • Paid vacation, holidays, and sick leave.
  • Medical, dental, and vision insurance for eligible employees.
  • 401(k) benefits for eligible employees.
  • Eligibility for long-term incentive programs.

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