Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Понятная роль в биостатистике у крупной компании дает возможность участвовать в ведении клинических исследований, но зарплата не указана, а широкий набор лидерских задач может быть непростым для специалиста с небольшим опытом.
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Широкая зона ответственностиЗарплата не указанаВостребованные технологииВлияние на медицину
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Biostatistician-KunTuo (Clinical Research/Statistical Analysis): Developing statistical analysis plans, datasets, tables, listings, figures, and clinical study reports for clinical trials with an accent on SAS programming, CDISC/ADaM standards, and regulatory compliance. Focus on validating complex deliverables, supporting database lock and unblinding, leading study-level statistical activities, and mentoring junior staff.
Location: Shanghai, China; other location: Beijing, China
Company
hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
Prepare statistical analysis plans and detailed specifications for datasets, tables, listings, and figures.
Program and validate datasets and TLFs using industry standards, checking logs, outputs, formats, content, and data issues.
Interpret analyses and author or review statistical sections of protocols, clinical study reports, and statistical reports.
Support study startup activities, including protocol development, sample size calculation, protocol review, and case report form review.
Lead or support study-level statistical activities, database lock, unblinding, randomization specifications, timelines, budgets, risk management, and client discussions.
Train and mentor junior staff and collaborate with project teams, data management, resource managers, clients, and other functions.
Requirements
Bachelor's or master's degree in biostatistics or a related field with 1–3 years of relevant experience, or a Ph.D. in biostatistics or a related field.
Intermediate knowledge of the principles, theories, and concepts of the job area, obtained through advanced education and experience.
Strong working knowledge of SAS and familiarity with relevant statistical computing packages such as StatXact.
Familiarity with moderately complex statistical methods applicable to clinical trials.
In-depth knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice and International Conference on Harmonization guidelines.
Working knowledge of relevant data standards, including Clinical Data Interchange Standards Consortium and ADaM.
Excellent written, oral, grammatical, and technical communication skills, with strong attention to detail and accuracy.
Strong initiative, organization, commitment to quality, and ability to manage multiple tasks and projects.
Ability to solve moderately complex problems, follow and provide direction, and establish effective relationships with coworkers, managers, and clients.
Culture & Benefits
Work in clinical research, life sciences, healthcare intelligence, and the development of medical treatments.
Collaborate with project teams, clients, data management, and cross-functional colleagues.
Participate in knowledge sharing, staff training, mentoring, and process improvement.
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