Study Design Statistician (Remote - Canada)

MMS

Toronto

Remote

CAD 110,000 - 160,000

Full time

4 days ago
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Job summary

MMS Holdings Inc is a data-focused clinical research organization seeking a Strategic Statistician. You will act as an internal and external SME for clinical trial design and provide broad statistical consultation to clients, leveraging KerusCloud for simulation and analysis.

You will lead the full statistical life cycle, collaborate with cross-functional teams, and contribute to pre-sales discussions while advancing methodological innovations within a global CRO environment.

Qualifications

  • Bachelor's degree in mathematics, statistics, physics, pharmacology or a strong statistical component; master's or PhD preferred.
  • 5–7 years of experience in medical statistics (pharma, CRO, academic).
  • Willingness to engage with clients to understand problems and provide solutions.
  • Experience 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; Bayesian approaches preferred.

Responsibilities

  • Lead the full life cycle of KerusCloud support and statistical services.
  • Assist customers with study design, focusing on simulation with KerusCloud.
  • Prepare study protocols and develop Statistical Analysis Plans and Statistical Analysis Reports.
  • Summarize, analyze and visualize study data using various statistical methods and deliver results on schedule.
  • Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party deliverables.
  • Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design; participate in CPD.
  • Support pre-sales discussions to understand client needs and contribute to technical solutions and cost estimates.
  • Collaborate with Product Development to define key features and statistical aspects of KerusCloud; support marketing with demonstrations and white papers.

Skills

Medical statistics
Client engagement
Statistical consulting

Education

Bachelor's degree in statistics/related field
Master's or PhD preferred

Tools

SAS
R

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team?MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

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 ourStrategic Statistical ServicesArm, this is a full-time role with emphasis on being an internaland externalSME for clinical trial design, together withproviding consultation to adviseclients on a range of broader statistical issues and will have an internal job title ofStrategic 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
  • Bachelor's degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, master's 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.
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