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4 дня назад

Senior Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)

117 000 - 184 200$
Формат работы
hybrid
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Релокация
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 Scientist, Statistical Programming, Late-Stage Oncology (Hybrid) (SAS/Clinical Trials): Developing and validating statistical analysis and reporting deliverables, datasets, and regulatory submission outputs for late-stage oncology drug and vaccine programs with an accent on SAS programming, CDISC/ADaM standards, and cross-functional project leadership. Focus on designing complex programming algorithms, coordinating global programming teams, and ensuring high-quality deliverables across the product lifecycle.

Location: Hybrid role based in North Wales, Pennsylvania, or Rahway, New Jersey, United States. Available to US, Canada, and Puerto Rico residents; domestic relocation is listed as available. Travel requirements: 10%.

Salary: $117,000–$184,200 annual base salary for the primary location, plus possible annual bonus and long-term incentive.

Company

hirify.global's BARDS organization applies quantitative science and research methodologies to support the discovery, development, regulatory approval, manufacturing, and marketing of medicines and vaccines.

What you will do

  • Develop and validate statistical analysis and reporting programs and deliverables, including safety and efficacy datasets, tables, listings, and figures.
  • Design and maintain statistical datasets supporting clinical development, outcomes research, and safety evaluation.
  • Serve as the statistical programming point of contact and knowledge holder across the product lifecycle.
  • Lead project-level programming activities, maintain project plans and resource forecasts, and coordinate global programming teams including outsource provider staff.
  • Collaborate with statistics and other stakeholders to deliver efficient, timely, and high-quality project outputs.
  • Contribute to departmental strategic initiative teams.

Requirements

  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or a related field plus at least 5 years of SAS programming experience in a clinical trial environment; or an MS in one of these fields plus at least 3 years of such experience.
  • Significant expertise in SAS and clinical trial programming, including data steps, procedures, SAS/MACRO, SAS/GRAPH, systems, and databases.
  • Experience developing analysis and reporting deliverables for R&D projects, including data, analyses, tables, graphics, and listings.
  • Experience with CDISC and ADaM standards, clinical data management concepts, process compliance, and deliverable quality.
  • Ability to design complex programming algorithms, understand analysis plans and statistical terminology, and anticipate stakeholder requirements.
  • Project-level leadership skills, independent task completion, and effective collaboration with key stakeholders.
  • Effective interpersonal, negotiation, written, oral, presentation, and collaboration skills.
  • Strategic thinking with the ability to turn strategy into tactical activities and design statistical databases that optimize analysis and reporting.

Nice to have

  • Experience with GenAI tools such as Python, R, R Shiny, or Claude.
  • Experience with regulatory submissions and electronic submission deliverables for US or worldwide drug or vaccine applications.
  • Experience directing other programmers, mentoring, and ensuring programming consistency across protocols and projects.
  • Experience completing deliverables through global outsource programming staff and managing project plans with Microsoft Project or a similar tool.
  • Experience with SDLC, reporting processes, process improvement, professional societies, and working across cultures and geographies.

Culture & Benefits

  • Hybrid work arrangement with regular collaboration across global teams.
  • Comprehensive medical, dental, vision, insurance, retirement, 401(k), paid holiday, vacation, compassionate, and sick-day benefits.
  • Inclusive workplace focused on diverse perspectives, respectful challenge, and collective problem-solving.
  • Regular employee status with possible annual bonus and long-term incentive eligibility.

Hiring process

  • Applications are accepted through the hirify.global careers portal; current employees and contingent workers have separate application routes.
  • Accommodation support is available during the hiring process for eligible applicants.

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