Statistical Scientist Job Locations United Kingdom-London | United Kingdom-Stirling Category Data Management & Statistics Overview
Medpace is a scientifically-driven, global, full-service clinical contract research organisation (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 3,000 people across 40 countries. Job Summary Due to continuous business growth, we are expanding our Global Biostatistics team, and looking for a full-time Statistical Scientist to join our office-based team in Central London.
This role is responsible for leading the Biostatistics activities for multiple complex clinical trial projects, working directly with the client and collaborating with other departments and Clinical Trial Management team, operating in a leadership position and representing the Biostatistics department at client meetings.
This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities Development of detailed Medpace Data Analysis Plan for assigned projects; Development of analysis databases; Communication of project requirements for CRF design, database design, and database clean-up to ensure the key study variables are suitable for analysis; Programming of study analysis, review of study results, and preparation of statistical methods section for clinical/statistical reports, and related regulatory submission documents; Communication of statistical results to medical writing personnel to ensure accurate interpretation; and Collaboration with Global Statistics team members and programmers to ensure study outputs are produced to a high quality and in a timely fashion. Qualifications Master’s Degree in statistics, biostatistics, or equivalent areas and strong relevant industry or equivalent experience; Significant SAS Programming experience; Excellent communication and leadership skills; Familiarity with regulatory requirements/guidelines for data submission and analysis; Expertise in biostatistical methodologies applicable to Clinical Trials; and Knowledge of advanced programming methods. Why Medpace? When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Awards Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer Winner of the ACRP-Avoca CRO Quality Award in 2018 Recognized with six CRO Leadership Awards from Life Science Leader magazine Eagle Award winner – which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships
What to Expect Next
We look forward to receiving your application. A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.
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