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Biostatistician PhD

Published 2025-03-31

Overview

Biostatistician - PhD

UK Remote

The Emmes Company, LLC (“Emmes”) is a global, full-service Clinical Research Organization dedicated to excellence in supporting the advancement of public health and biopharmaceutical innovation. We believe in the power of truth, so much so that we named our company Emmes, which means truth. Through decades of experience we have learned that collaborative relationships thrive and human health benefits when truth is our compass.

Our “Character Achieves Results” culture is driven by five key values that guide our actions in the way we conduct research and distinguish us as an organization: Integrity, Agility, Passion for Excellence, Collaborative Partnerships and Intellectual Curiosity. We are a trusted partner to clients who share our passion for improving public health in a world of ever-changing scientific research.

If you share our motivations and passion in research, come join us! You will be joining a collaborative culture that empowers every Emmes employee — from entry level through top executive — to contribute to our clients’ success by sharing ideas openly and honestly.

Primary Purpose

The Biostatistician collaborates with clinical investigators to determine study design, contributes to protocol development, writes statistical analysis plans, performs statistical analysis and inference and writes and presents reports summarizing findings including publications in peer-reviewed journals. The Biostatistician develops systems for monitoring the quality of clinical data. The Biostatistician ensures high-quality statistical support is provided for clinical trials, registries and basic research using advanced statistical skills and knowledge of clinical research. The Biostatistician maintains expertise in state-of-the-art data manipulation and statistical methodology.

Responsibilities

Collaborates with clinical investigators to determine study design

Writes sections of protocols that require statistical input

Reviews protocols and case report forms to ensure that protocol objectives are met and standards are maintained

Generates treatment allocations in randomized clinical research studies and ensures proper implementation

Leads the project team’s development of statistical analysis plans and programs to perform analyses and display study data

Performs statistical analyses, writes and validates application programs

Implements data and safety monitoring reports to ensure participants safety

Develops metrics and generates quality control reports to optimize the performance of clinical sites and the coordinating center

Generates study reports to be distributed to internal and external monitoring committees and regulatory bodies

Authors or contributes to manuscripts and/or scientific presentations

Participates in professional development activities both within and outside the company