Senior Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
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
'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 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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