Study Design Statistician (Remote)
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 31d ago
The date the source published, not the day we noticed it (2026-10-02). Last seen at its source 2h ago.
We have tracked this listing since 18 Oct 2026 (15 days). The employer's own board has carried it every time we have read it, most recently 2 hours ago.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
United States
The description states no restriction of its own. This is the source's own tag.
Pay not stated
Similar roles pay $121.9k–210k/yr
Middle 50% of 372 listings that do state pay — Design · all levels · United States · USD/year. This employer has published no salary; this is what comparable listings we hold disclose, never converted between currencies or periods. How this is calculated.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
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JazzHR employer's own board first seen 15d ago · last seen 2h ago
The listing
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
As part of our Strategic Statistical Services Arm, this is a full-time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician.
Job Description:
Our experienced statisticians and programmers develop intellectual property and assets to support the design and analysis of clinical trials, precision medicine and real-world data analytics. We address the emerging analytics needs of the Industry with our biostatistics services, bespoke algorithms and unique, state of the art, proprietary, cloud-based trial simulation software KerusCloud. Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from:
- Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives.
- Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports.
- Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality.
- Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables.
- Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity.
- Support pre-sales discussions to understand and identify client needs, then contribute to technical solutions and resource/ cost estimates.
- Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud.
- Provide input and support to Marketing of KerusCloud, including demonstrations to clients, white papers, etc.
Requirements:
- Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred.
- 5-7 years of experience in the application of medical statistics (pharma, CRO, academic).
- Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions.
- Experience in delivering customer projects to high quality standards.
- Experience in SAS and/ or R statistical software packages.
- Experience in study design and protocol and report-writing preferred.
- Experience of modelling and simulation techniques to explore complex study designs preferred.
- Experience of Bayesian approaches to design and analysis of clinical data preferred.
- Experience of early-phase drug development processes including innovative/ adaptive study design preferred.