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Зарплата не указанаАктуальные инструментыПонятные задачиКрупный работодатель
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Описание вакансии
Текст:
Hirify AI/Оригинал
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 clinical research standards, data validation, and moderately complex statistical methods. Focus on leading statistical activities, managing database lock and unblinding processes, mentoring junior staff, and controlling study quality, timelines, and budgets.
Location: Taipei, Taipei City, Taiwan
Company
Clinical research, commercial insights, and healthcare intelligence services support the development and commercialization of medical treatments and improvement of patient outcomes.
What you will do
Prepare statistical analysis plans and detailed programming specifications for datasets, tables, listings, and figures.
Program and validate datasets and statistical outputs, review logs, resolve data issues, and ensure deliverable quality according to SOPs.
Interpret analyses and draft or review statistical sections of clinical study reports and protocols.
Lead statistical activities on assigned studies, coordinate with project teams and customers, and provide progress, timeline, resource, and budget input.
Support data management, database design, validation checks, database lock, unblinding, randomization, protocol development, and sample size calculations.
Train and mentor junior staff, identify delivery risks, and contribute to cross-functional collaboration and knowledge sharing.
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.
In-depth knowledge of applicable clinical research regulatory requirements, including Good Clinical Practice and International Conference on Harmonization guidelines.
Familiarity with moderately complex statistical methods applicable to clinical trials.
Strong working knowledge of the SAS computing package and working knowledge of relevant data standards such as CDISC and ADaM.
Familiarity with relevant statistical computing packages such as StatXact.
Excellent written and oral communication, grammatical and technical writing, attention to detail, accuracy, organization, and commitment to quality.
Ability to manage multiple tasks and projects, solve moderately complex problems, provide and accept direction, and maintain effective working relationships with coworkers, managers, and clients.
Nice to have
Experience contributing to proposals, budgets, request-for-proposal responses, or bid defenses.
Experience serving as a primary customer contact or consulting with clients on operational topics.
Culture & Benefits
Work is conducted within a global clinical research and healthcare intelligence organization.
Responsibilities include knowledge sharing, mentoring, cross-functional collaboration, and support for colleagues.
Work emphasizes integrity, quality, proactive risk management, and effective communication.
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