8 дней назад
Senior Statistical Programming Lead (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
Senior Statistical Programming Lead (SAS): Planning and leading programming activities for complex clinical trials, including statistical analysis, reporting, and CDISC-compliant submission packages with an accent on SAS programming, clinical data standards, and cross-functional delivery. Focus on coordinating teams and vendors, guiding complex data workflows, implementing metadata-driven efficiencies, and ensuring high-quality regulatory submissions.
Location: Shanghai, China
Company
Johnson & Johnson MedTech develops healthcare and medical technology solutions designed to improve prevention, treatment, and patient outcomes.
What you will do
- Plan programming strategy, coordinate activities, and oversee execution for clinical trials and projects.
- Design and develop programs for complex clinical data analysis and reporting.
- Create, verify, and deliver CDISC-compliant and non-standard submission data packages and reviewer’s guides.
- Provide technical guidance to programming teams and ensure timely, high-quality deliverables.
- Collaborate with clinical, statistical, regulatory, data management, vendor, and other cross-functional stakeholders.
- Lead process, system, technology, and metadata-driven improvement initiatives, including oversight of outsourced programming work.
Requirements
- Bachelor’s degree or equivalent technical depth in computer science, mathematics, data science, data engineering, public health, or a related scientific field.
- Approximately 4+ years of programming or clinical data management experience, preferably in pharmaceutical or clinical trial environments.
- Knowledge of SAS is required; experience with R, Python, or other programming languages for data manipulation, statistical analysis, and reporting is relevant.
- Expert knowledge of CDISC standards and working knowledge of ICH-GCP and clinical research and development concepts.
- Experience planning and coordinating programming activities, leading teams, managing vendors, and working with cross-functional stakeholders.
- Strong written and verbal communication, project management, data quality, and quality assurance skills.
Culture & Benefits
- Inclusive work environment focused on respecting diversity, dignity, and individual contribution.
- Opportunity to contribute to healthcare innovation and clinical development programs.
- Collaboration with internal functions, external partners, CROs, vendors, and industry working groups.
- Full-time employment within the Innovative Medicine and MedTech organization.
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