Statistical Scientist

Created by: Medpace
Added: 24.07.2020

Advert description

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 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.

Specific details

Type of Contract Full time
Preferred Education Master's, Other
Level of Experience 5-10 years

Location

United Kingdom, Europe
London