Biostatistician

Created by: Medpace
Added: 03.01.2020

Advert description

Overview

 

Medpace is a scientifically-driven, global, full-service clinical contract research organization (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

Biostatistician - PhD

 

Permanent, full-time, office-based in Central London

Salary - Competitive

 

Due to continuous business growth, we are expanding our Biostatistics team, and looking for a full-time Biostatistician to join our office-based team in Central London. This position will work in a team to accomplish tasks and projects that are instrumental to the company’s success.

 

This role is responsible for Biostatistics activities for clinical trial projects; to ensure that work is completed within the defined time frames to appropriate quality levels, and present the Biostatistics function at conferences, external non-study meetings and bid defense meetings. If you want an exciting career where you can use your previous expertise and develop and grow your career even further, then this is the opportunity for you.

 
Responsibilities

  • Contribute to clinical development of plan preparation;
  • Review of study protocol and preparation of statistical methodologies;
  • Development of detailed Data Analysis Plan for assigned projects;
  • Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;
  • Communicate project requirements for CRF design, database design and database clean-up to ensure the key study variables are suitable for analysis; and
  • Communicate statistical results to medical writing personnel to ensure accurate interpretation.

Qualifications

 

  • Ph.D. degree in Biostatistics / Statistics with strong experience in SAS Programming or equivalent;
  • Knowledge of advanced statistical methods and knowledge of the pharmaceutical industry;
  • Knowledge of regulatory requirements/guidelines for drug development; and
  • Previous experience in a pharmaceutical or CRO setting desirable.

 

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.

EO/AA Employer M/F/Disability/Vets

  • WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process

Specific details

Type of Contract Full time
Preferred Education Master's
Level of Experience 2-5 years

Location

United Kingdom, Europe
London