GSKPrincipal Statistician
GSK is hiring a Principal Statistician in Tokyo, Japan. Level rates it ; you can apply on GSK.
Level's read on this job
- Little AI ●○○○ is how Level rates this role: aI is not part of the work.
- The posting allows some remote work.
- Tools and skills the posting cites include Bayesian Methods, statistical analysis and clinical trials.
- Level lists 1,000+ other open roles at GSK.
- The role was posted within the past two weeks.
AI in this role
Lead statistical planning and clinical trial design for healthcare research projects in Japan.
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Our approach to R&D Position Summary You will lead statistical planning and delivery for clinical research in Japan. You will work with cross-functional teams to design trials, analyse data, and support regulatory interactions. We value clear scientific thinking, pragmatic problem solving, and a genuine focus on patients. You will grow technical and leadership skills while helping bring research advances to people who need them. Join us to use your statistical expertise to make a measurable difference and to develop your career in a supportive, mission-driven environment. Responsibilities This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: - Act as the primary statistical lead for Japan projects, contributing to study design, analysis plans, and interpretation of results. - Collaborate with global statisticians and local cross-functional teams to align trial design and analysis across regions. - Prepare statistical input for regulatory interactions and support submissions to Japanese health authorities. - Oversee external statistical partners and vendors to ensure quality, timelines, and cost control. - Apply modern statistical methods, including adaptive and Bayesian approaches when appropriate, to enable efficient and ethical study designs. - Coach and mentor statisticians and non-statistical colleagues, promoting good statistical practice and reproducibility. Why You? Basic Qualification We are seeking professionals with the following required skills and qualifications to help us achieve our goals: - Degree in statistics, biostatistics, mathematics or a closely related quantitative discipline. - At least 5 years of experience working as a statistician in randomized clinical trials, with industry or CRO experience. - Practical experience in clinical trial design and statistical analysis. - Proficiency with statistical software such as R or SAS and working knowledge of clinical trial data formats and conventions. - Business-level English and fluent Japanese (ability to read, write and speak in Japanese at professional level). - Strong communication skills with experience explaining statistical concepts to non-statisticians. Preferred Qualification If you have the following characteristics, it would be a plus: - PhD or advanced degree in statistics, biostatistics, or related field. - Experience with regulatory submissions and direct interactions with Japanese regulatory authorities. - Knowledge of adaptive designs, Bayesian methods, or other innovative statistical approaches. - Background in one or more therapeutic areas relevant to our work in Japan. - Experience managing external vendors and contract statisticians. - Familiarity with data science tools and modern workflows oriented to reproducibility and automation. Working Arrangement This role is hybrid, based in Japan, combining on-site work with flexible remote days as agreed with the line manager. Some travel within Japan and occasional international collaboration may be required. What you will bring You bring strong statistical judgement and the ability to make clear recommendations. You enjoy working with diverse teams and communicating results in simple, actionable terms. You work with integrity and focus on patient impact. You welcome feedback and support the growth of others. How to apply If this role fits your experience and ambitions, we encourage you to apply. Please submit your CV and a short cover note describing a statistical project you led and the impact it delivered. We will review applications and contact candidates for next steps. We are committed to inclusion. We welcome applications from people with different backgrounds, experiences and perspectives.
Skills
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
We are committed to creating an inclusive workplace and providing equal opportunities for all applicants. We embrace an agile working culture across our roles, so if flexibility is important to you please discuss opportunities with our hiring team. If you need any adjustments to the recruitment process to help you demonstrate your strengths and capabilities, contact APACRecruitment.Adjustments@gsk.com. Please note this email is for adjustment requests only; for other enquiries please use our standard contact channels.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.
How we rate this
Principal Statistician at GSK rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.
Little AI. AI is not part of the work.
- ●●●● Builds AI80 to 100
- ●●●○ Works on AI60 to 79
- ●●○○ Uses AI40 to 59
- ●○○○ Little AI0 to 39
Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.
Prepare for this job
Built from this posting and from similar jobs on Level.
Skills and AI tools this role asks for
Questions you could be asked
- Tell me about a project where statistical analysis was part of your work. What did you do?
- Tell me about a project where clinical trials was part of your work. What did you do?
- Tell me about a project where study design was part of your work. What did you do?
- Tell me about a project where regulatory submissions was part of your work. What did you do?
- Tell me about a project where biostatistics was part of your work. What did you do?
Adapt your resume
- List these exact terms on your resume: Statistical Analysis, Clinical Trials, Study Design, Regulatory Submissions, and Biostatistics. An applicant tracking system matches the wording, not the idea.
- Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.
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