• Data Programmer

    Job Locations - | Germany-Berlin
    Posted Date 1 month ago(6/6/2018 10:59 AM)
  • Overview

    At PRA, we don’t make our 15000+ people great. It’s the other way around. As we have grown to a top-5 CRO, we have maintained the feel of a small company, dedicated to collaboration and passion for what we do.


    We always have a desire to keep seeking new and better ways to operate. We don’t settle for the same old ways. Our passion for improving patient lives worldwide permeates all that we do. Put simply, we care.


    The Early Development Services (EDS) division of PRA is a global leader in providing early-phase clinical research and bioanalytical services to the pharmaceutical and biotechnology industries. With a reputation built on excellence, quality and professionalism, we work with leading pharmaceutical and biotechnology companies, performing clinical research and bioanalytical trials on many of the most advanced experimental drugs and biologics in development today. Employees of EDS are enthusiastic and dedicated and work in a dynamic informal organization.


    Patient Pharmacology Services is a group within EDS focusing on early-phase clinical trials in patient populations. With management offices in Germany, and clinical operations in several cities across Central Europe, we now have an opening for an experienced Data Programmer to join the team in our Berlin offices.


    As an experienced programmer you will be responsible for accessing and assembling clinical data from a variety of sources, converting the data to tabulation datasets and creating derived datasets following industry and client specifications.


    Duties such as: generating tables, figures and listings to support analysis.  A solid understanding of with CDISC data standards (SDTM and ADaM), creating annotated case report forms and documenting datasets including define.xml files will be a crucial element of the job


    Applicants need to be familiar with the study protocol and the statistical analysis plans of assigned projects to ensure study tasks are completed in accordance with clinical trial documentation.


    You are:


    Delivery focused and an innovative leader.

    Here at PRA we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:

    What do you bring as Clinical Programmer?

    • An undergraduate degree (Bachelor or Master degree) in a quantitative or scientific field, e.g. Mathematics, Medical Documentation, Bio (Medical) Sciences with a proven preference for analytical thinking and programming
    • Excellent written and oral communication in English
    • Experience with Clinical Programming and preferably understanding of the SAS language
    • Knowledge of CDISC-standards
    • Attention to detail
    • Preferably experience in statistical evaluations of clinical data

    You will be frequently collaborating within multi-cultural global teams, so will need to demonstrate excellent written and oral communication skills, exhibit pro-active teamwork alongside a positive attitude, and maintain up-to-date industry awareness and understanding of regulation/standards.


    Your health, your family, your career, your money — the things that matter to you, matter to us. The benefits of PRA just get better and better.


    PRA Health Sciences is an Equal Opportunity Employer. We welcome and encourage diversity in the workplace.


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