Study Design Statistician

Responsibilities

• Serve as a subject matter expert for clinical trial design, providing statistical consultancy to sponsors across the clinical development spectrum.
• Lead the full life-cycle of KerusCloud support and statistical services, including assisting customers with study design and simulation.
• Prepare study protocols and develop Statistical Analysis Plans (SAPs) and Statistical Analysis Reports (SARs).
• Summarize, analyze, and visualize study data using various statistical methods to deliver high-quality results on agreed timelines.
• Support pre-sales discussions by identifying client needs and contributing to technical solutions and cost estimates.
• Collaborate with the Product Development team to define key features and statistical aspects of KerusCloud.
• Provide input to Marketing efforts, including client demonstrations and the development of white papers.

Requirements

• Bachelor's degree in mathematics, statistics, physics, pharmacology, or a related field with a strong statistical component.
• 5-7 years of experience in the application of medical statistics within pharma, CRO, or academic environments.
• Proficiency in SAS and/or R statistical software packages.
• Proven ability to engage with clients to research problems and provide creative, business-oriented solutions.
• Experience delivering customer projects to high-quality standards.

Preferred Qualifications

• Master's or PhD degree.
• Experience in study design, protocol writing, and report writing.
• Knowledge of modeling and simulation techniques to explore complex study designs.
• Experience with Bayesian approaches to the design and analysis of clinical data.
• Experience with early-phase drug development processes, including innovative or adaptive study designs.

About the Company

MMS is an award-winning, data-focused clinical research organization (CRO) that supports the pharmaceutical, biotech, and medical device industries. Recognized as a Great Place to Work, MMS fosters a collaborative and inclusive environment with a global footprint across four continents. We specialize in addressing complex trial data and regulatory submission challenges through a scientific approach and state-of-the-art proprietary technology.