Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Хорошая вакансия
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Обязанности хорошо очерчены, а работа дает возможность самостоятельно вести программирование онкологических исследований. Но без зарплаты и подробностей контракта сложно оценить общую привлекательность условий.
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Зарплата не указанаАктуальный инструментарийЧеткая зона ответственностиРазработка лекарствОбучение и наставничество
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Statistical Programmer/Analyst Consultant (Oncology) (SAS/CDISC): Leading statistical programming for oncology clinical studies from study start-up through database lock, analysis, and reporting with an accent on SAS programming, CDISC-compliant SDTM and ADaM datasets, and clinical trial reporting. Focus on developing and validating TLFs, supporting regulatory submissions, independently managing programming deliverables, and mentoring junior programmers.
Location: Remote in the United States
Company
hirify.global 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 statistical programming activities for oncology clinical studies from study start-up through database lock, analysis, and reporting.
Develop, review, and maintain SAS programs for SDTM, ADaM, tables, listings, and figures.
Lead interim and final efficacy and safety analyses and support regulatory submissions.
Develop and review programming specifications in alignment with protocols, statistical analysis plans, and study methodology.
Generate and validate clinical trial outputs, datasets, and clinical study report deliverables.
Coordinate study-level programming activities, communicate risks and timelines, and mentor statistical programmers.
Requirements
Must be based in the United States; remote work is available within the US.
Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field.
Significant experience in oncology clinical trials and strong experience in clinical trial statistical programming.
Strong proficiency in SAS, including Base SAS and procedures used for clinical trial reporting.
Strong knowledge of CDISC standards, particularly SDTM and ADaM, with experience developing and validating TLFs.
Experience with complex clinical trial data, regulatory submissions, independent programming delivery, and cross-functional collaboration.
Nice to have
Basic or working knowledge of R programming.
Experience in a CRO, pharmaceutical, or biotechnology environment.
Culture & Benefits
Work directly with a single sponsor while receiving the support and career opportunities of a global CRO.
Professional development supported through continuous training and mentorship.
Client-facing work with an emphasis on independent ownership and high-trust collaboration.
Inclusive workplace with a focus on diversity and equal opportunity.
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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