5 дней назад
Biostatistical Programming Senior Associate (SAS)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Biostatistical Programming Senior Associate (SAS): Developing and validating statistical programs, clinical trial datasets, tables, listings, and figures for safety and efficacy analyses and regulatory submissions with an accent on CDISC standards, clinical data quality, and complex statistical programming. Focus on analyzing clinical trial data, preparing submission documentation, and collaborating with globally dispersed study teams across therapeutic areas.
Location: Taipei, Taiwan
Company
is a biotechnology company developing and delivering innovative human therapeutics through global research, manufacturing, and support capabilities.
What you will do
- Analyze and report clinical trial data using SAS and/or R.
- Create and validate complex SDTM, ADaM, safety, and efficacy datasets.
- Create and validate complex tables, listings, and figures.
- Prepare statistical programming specifications, regulatory submission documents, and validation tracking documentation.
- Develop and validate programs for data quality checks while collaborating with cross-functional and global study teams.
- Support or provide backup for the Study Lead Programmer.
Requirements
- At least 4 years of statistical programming experience in a clinical development environment.
- Bachelor’s degree or higher in biostatistics, statistics, mathematics, computer science, or a related quantitative or scientific field.
- Experience manipulating, analyzing, and reporting complex clinical trial data, with familiarity with the drug development lifecycle.
- Working knowledge of CDISC SDTM and familiarity with CDISC ADaM and Define standards.
- In-depth knowledge of SAS/STAT packages and familiarity with data quality and compliance-checking tools.
- Excellent oral and written English communication skills and the ability to work with globally dispersed, cross-cultural teams.
Nice to have
- Master’s degree or higher in statistics, biostatistics, mathematics, or a related field.
- Experience with R, Python, automation platforms, or emerging statistical programming technologies.
- Prior regulatory submission experience for drug approval.
Culture & Benefits
- Opportunities to learn and advance across a global organization.
- Diverse and inclusive workplace where employees are empowered to contribute ideas and take action.
- Total rewards package covering health, financial and wealth, work-life balance, and career benefits.
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