3 дня назад
Senior Statistical Programmer (SAS/R)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Statistical Programmer (SAS/R): Leading statistical programming for clinical trials, including validated datasets, tables, figures, listings, and CDISC-compliant electronic submissions with an accent on SAS, R, clinical data standards, and cross-functional delivery. Focus on overseeing programming deliverables, supporting SDTM/ADaM specifications, managing vendors, and providing technical guidance to other programmers.
Location: United States; remote role
Company
is a global full-service contract research organization providing clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.
What you will do
- Lead and support statistical programming activities for clinical trials.
- Program and validate derived datasets, tables, figures, and listings using clinical trial data and external data sources.
- Program and validate CDISC-compliant deliveries and support electronic submission documentation.
- Contribute to CRF, Data Transfer Specification, Statistical Analysis Plan, SDTM, ADaM, and Define package development and review.
- Oversee programming deliverables from CROs, internal contractors, and external vendors while ensuring timely, high-quality delivery.
- Develop working instructions, guidelines, enhanced functions, macros, and utilities.
Requirements
- Bachelor’s or master’s degree in Computer Science, Mathematics, Engineering, Medical, or a related discipline.
- More than 5 years of statistical programming experience with a bachelor’s degree, or 3 years with a master’s degree, in the pharmaceutical industry.
- Strong SAS and SAS Macro language skills, with working knowledge of SAS components.
- Knowledge of R programming in clinical trials and familiarity with the drug development process.
- Strong knowledge of industry standards and experience with data integrations such as ISS and ISE.
- Strong oral and written communication skills, including the ability to explain analyses to less technical colleagues.
Culture & Benefits
- Permanent position within an in-house team.
- Projects supporting pharmaceutical, biotechnology, medical device, and consumer health clients.
- Professional growth supported by continuous training and development.
- One-team, quality-driven culture focused on diversity and inclusion.
- Opportunity to contribute to the development and commercialization of innovative drugs and devices.
Hiring process
- Submit a CV and receive an application acknowledgement.
- Qualified candidates are invited to a phone interview as the first step.
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