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4 дня назад

Biostatistician 2

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
China/Taiwan
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 2 (SAS/Clinical Trials): Preparing statistical analysis plans, programming datasets and tables, listings, and figures, and contributing to clinical study reports with an accent on CDISC/ADaM standards, GCP/ICH requirements, and statistical quality control. Focus on leading statistical activities, managing database lock and unblinding processes, solving data and delivery risks, and mentoring junior staff.

Location: Shanghai, China; other available locations include Beijing, China and Taipei, Taipei City, Taiwan.

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 statistical outputs according to SOPs and industry standards, reviewing logs, data issues, formats, and content.
  • Interpret analyses and author or review statistical sections of protocols, clinical study reports, and statistical reports.
  • Lead statistical activities on assigned studies, collaborate with project teams and customers, provide progress updates, and manage timelines, resources, scope, and budgets.
  • Support data management, database design, validation checks, critical data review, database lock, unblinding, randomization, and study start-up activities.
  • Identify delivery and quality risks, propose mitigation solutions, train staff, mentor junior colleagues, and support cross-functional collaboration.

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 biostatistics, with familiarity with moderately complex statistical methods used in clinical trials.
  • In-depth knowledge of applicable clinical research regulations, including Good Clinical Practice and International Conference on Harmonization guidelines.
  • Strong working knowledge of SAS and familiarity with relevant statistical computing packages such as StatXact.
  • Working knowledge of relevant data standards, including CDISC and ADaM.
  • Excellent written and oral communication, grammatical and technical writing skills, attention to detail, and accuracy.
  • Strong initiative, organizational skills, commitment to quality, and ability to manage multiple tasks and projects.
  • Ability to solve moderately complex problems, provide and accept direction from lead team members, and build effective relationships with coworkers, managers, and clients.

Culture & Benefits

  • Full-time employment within a global clinical research and healthcare intelligence organization.
  • Collaboration with project teams, customers, data management, and cross-functional colleagues.
  • Opportunities to train staff, mentor junior colleagues, and contribute to operational knowledge sharing.

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