Overview/About Lumanity
Lumanity is dedicated to improving patient health by accelerating and optimizing access to medical advances. We partner with life sciences companies worldwide to:
Our work spans three complementary areas: Strategy & Insights, Value, Access & Outcomes, and Medical Strategy & Communications.
Responsibilities / Position overview
About the role
The Patient-Centered Outcomes (PCO) team at Lumanity is seeking a Statistician to join our growing statistics group. This position can be based in the US (preferred), with flexible working arrangements; UK or EU considered.
We are looking for candidates with a proven track record in life sciences consulting and expertise in applying advanced statistical methods to patient-reported outcomes (PROs).In this role, you will:
This is a career-growth opportunity, with the hiring title determined by experience. You will start by contributing statistical expertise under the guidance of senior leaders, progressing to independently managing the full research pipeline, from study design through data analysis to final reporting.
Core Job Responsibilities
Scientific Leadership & Study Execution
Qualifications
Qualifications
Education & Experience: Master's degree or higher in Statistics or Biostatistics, with 3-5 years of experience in a life sciences consultancy.
Statistical Expertise for PROs: Proficiency in methods tailored for skewed, bounded, longitudinal, and missing PRO data, including:
Mixed Models for Repeated Measures (MMRM)
Analysis of Covariance (ANCOVA)
Logistic Regression
Non-parametric tests (e.g., Wilcoxon Rank-Sum)
Multiple Imputation or likelihood-based methods for missing data
Sensitivity analyses for post-hoc scenarios
Regulatory Knowledge: Comprehensive familiarity with frameworks that guide statistical methods for PROs, including:
FDA's Patient-Focused Drug Development Guidance Series and disease-specific guidances
HTA Coordination Group JCA Dossier guidance
EMA's Reflection Paper on patient experience data
ICH E9(R1) Statistical Principles for Clinical Trials: Addendum on Estimands and Sensitivity Analysis
FDA's 2017 draft guidance on Estimands in Clinical Trials
Technical Skills:
Proficiency in R, including packages for longitudinal and categorical data analysis, and the wider tidyverse suite
Experience working in a regulated programming environment
Documentation & Reporting: Skilled in preparing statistical analysis plans and technical reports using standardized templates to ensure efficiency and consistency.
Soft Skills:
Exceptional written and verbal communication skills, with the ability to translate complex statistical concepts into clear, actionable insights for diverse audiences
Strong problem-solving abilities and adaptability in fast-paced environments
Skilled in partnering with clients during high-stakes projects, balancing responsiveness with scientific rigor
Proven ability to collaborate respectfully and effectively within cross-functional, mixed-methods research teams
Innovation: Experience leveraging emerging AI tools to scale statistical programming and enhance scientific writing efficiency.
Benefits
We offer our employees a comprehensive benefits package that focuses on what matters to you - health and well-being, personal finances, professional development, and a healthy work/life balance:
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