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7 дней назад

Scientist, Statistical Programming, Early-Stage Oncology (Hybrid)

96 200 - 151 400$
Формат работы
hybrid
Тип работы
fulltime
Грейд
junior
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
Scientist, Statistical Programming, Early-Stage Oncology (Hybrid) (SAS/R and clinical development): Developing, validating, and maintaining efficacy and safety datasets, tables, listings, figures, and submission deliverables for early-stage oncology clinical trials with an accent on SAS programming, CDISC standards, and statistical reporting. Focus on validating analysis outputs, collaborating with statistics and outsourcing partners, and delivering compliant programming work under senior guidance.

Location: Hybrid; primary location in North Wales (Upper Gwynedd), Pennsylvania, USA. The role is available in two locations and is limited to residents of the United States, Canada, and Puerto Rico.

Salary: $96,200–$151,400 annual base salary for the primary location; annual bonus and long-term incentive may also apply.

Company

hirify.global develops medical drugs and vaccines through research and development activities supporting discovery, clinical development, regulatory approval, manufacturing, and global human health.

What you will do

  • Develop, validate, and maintain efficacy and safety datasets, tables, listings, and figures at the protocol level.
  • Prepare statistical analysis and reporting datasets, outputs, and submission deliverables for early-stage oncology clinical development projects.
  • Perform validation according to departmental SOPs and good programming practices.
  • Collaborate with statistics, project stakeholders, and outsourced providers on medical monitoring reports, requirements, validation, and deployment.
  • Gather and document user requirements for statistical programming deliverables.

Requirements

  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering, or a related field, plus a minimum of 2 years of SAS programming experience in a clinical trial environment; alternatively, an MS in one of these fields or a related field.
  • SAS programming experience with data steps, procedures, SAS/MACRO, and SAS/GRAPH.
  • Knowledge of CDISC SDTM and ADaM standards.
  • Knowledge and experience developing data, analyses, tables, graphics, and listings for R&D projects.
  • Ability to learn new programming techniques and data structures quickly and effectively.
  • Ability to take direction, complete project-level programming tasks under the guidance of a senior programmer, and collaborate with key stakeholders and project team members.
  • Good interpersonal, negotiation, written, oral, and presentation skills.
  • Interest in advancing through development activities and taking on increasingly challenging responsibilities.

Nice to have

  • R programming experience, including data derivation and analysis.
  • Knowledge of pharmaceutical development processes and clinical endpoint data, including efficacy and safety.
  • Unix operating system experience and systems or database experience.
  • Good working knowledge of reporting processes, SOPs, and the software development life cycle.

Culture & Benefits

  • Hybrid work arrangement.
  • Comprehensive medical, dental, vision, and other insurance benefits for employees and families.
  • Retirement benefits including a 401(k).
  • Paid holidays, vacation, compassionate leave, and sick days.
  • 10% travel requirement.
  • Inclusive environment focused on collaboration, diverse perspectives, and collective problem-solving.

Hiring process

  • Applications are accepted through the hirify.global careers portal.
  • The posting is effective until 11:59 PM on October 29, 2026.

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