Introduction

Introduction

We are currently hiring a Statistical Programmer (full-time, remote) for our client, a global pharmaceutical company and one of the largest pharmaceutical companies in the world. The company is known for its success in researching developing and marketing innovative drugs.

The Statistical Programmer will be responsible for the development of SAS programs and statistical output for the management and reporting of clinical trial data managed by the Unit. Ensure quality of statistical output produced by external provider, programs tools to support data review activities and data visualization and collaborate on the interpretation and communication of trial results. By contributing to regulatory submissions, converting of data according to regulatory requirements, preparation of integrated analyses and related documentation, the Statistical Programmer will play a strategic role in the Clinical Development Projects they are involved in. They will also support the development of standard operating procedures, performs post-hoc analysis for exploratory purposes, or supports regulatory requests, and prepares analysis for paper publications.

What are you going to do 

Responsibilities

  • To convert data to CDISC SDTM, following project specifications
  • To develop SAS programs to generate analysis datasets (CDISC compliant)
  • To produce datasets documentation according to CDISC and FDA requirements (define.xml) and/or to review analysis datasets documentation prepared by providers
  • To develop SAS programs to produce tables, listings, and figures as planned in the statistical analysis plan and to support data review activity before database lock
  • Develop SAS macros and SAS programs for data quality evaluation and to develop data quality reports
  • Writing, documenting, and performing quality control review of SAS programs
  • To perform ad hoc analysis for various statisticians’ requirements
  • To support statisticians in the preparation and/or review and QC of statistical package for FDA submissions
  • To perform QC of the programming material prepared by external providers guaranteeing the output provided is correct and in line with international requirements and with internal SOP/Standards

Essential skills and knowledge

Requirements

  • Bachelor's Degree in Statistics or Health Sciences/Computer Science is required
  • SAS certification and/or A. Stat or P. Stat accreditation are assets
  • 4+ years of experience in Pharma or CRO is required
  • Previous SAS experience and expertise is required
  • Previous experience with Data Management and Biostatistics processes.
  • In-depth understanding of CDISC standard
  • Proficient in MS Office (Word, Excel, Project, PowerPoint)
  • Proficient in relational databases

What we offer 

What We Offer

Why apply through Brunel? Finding the next step in your career can be a fulltime job in itself. We manage the process for you: from submitting your resume to coordinating interviews to extending offers and assisting with on-boarding. We’ll get you going while you get on with the job.

Are you the perfect match for this vacancy? Apply in 5 minutes and let's get in touch!

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Process of your application

Application process & contact

We will now begin examining your application: We will take a close look at your application documents and ask you for additional information if necessary. If your qualifications match our requirements, we will invite you to meet us for the first time.

Project discussion with our customer

If the introductory meeting goes well for you and us, we will arrange a meeting with the customer who has the perfect project for you. This gives you the opportunity to find out more about the customer and the project.

The decision

If you enjoyed the project discussion and the customer is also convinced of your expertise, we will ask you the final and decisive question: Do you want to get started at Brunel?

Introductory conversation with Brunel

In an introductory meeting, we would like to find out more about your interests, ambitions and professional developments. At the same time, we report on working at Brunel and provide information about all career opportunities and prospects.

Welcome to Brunel

Now great times are beginning! With Brunel you have countless opportunities to help shape technological progress. You decide how your career path goes. We support you in every phase of your career. You always have security behind you: Brunel!