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11 дней назад

Biostatistician-KunTuo

Формат работы
onsite
Тип работы
fulltime
Грейд
junior
Английский
b2
Страна
China
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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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