Statistical Programmer II

Discipline: Biometrics
Job type: Permanent
Salary: ££39000 - £43000
Contact name: Ashley Clarke

Contact email: ashley.clarke@rbwconsulting.com
Contact phone: +44 1293 584 300
Job ref: 23595
Published: 23 days ago
Expiry date: 22 May 2022

Statistical Programmer II

I am currently recruiting for a specialist contract research organisation (CRO) to the pharmaceutical industry. They are a niche company that provide programming and high quality statistics for the reporting of phases I – IV clinical trials. They have a presence in UK and Europe markets and due to their high standards and reputation are looking to expand further.  The role is permanent and candidates can be based In UK or In Europe and will be able to work from home.

This is a fantastic opportunity to develop your programming skills within a growing, specialist biomathematical services organisation. We welcome the right applicants from any industry with a willingness to develop their skills in our sector. You will receive continued support and a varied experience with complex and challenging projects, enabling you to progress your career and personal development.

Job profile

The role is primarily to complete programming activities to support our clinical trials clients but will also include data preparation and analysis of clinical and other biomathematical data with medium to high complexity. Duties will include the creation of datasets, tables, listings and figures according to project specifications and industry standards.

You will use and develop your programming skills in a data driven environment. Your responsibilities will include:

  • Development and documentation of programs used in the production of computer generated outputs for clinical study reports, registration and submission documents, plus any other document used to present clinical trials data, including specification and delivery of integrated databases, outputs and response to regulatory questions; commercialisation and reimbursements
  • Development of standard methodology to improve quality, efficiency and effectiveness

 

Experience

 

  • Experience programming in SAS, including writing SAS macros in a clinical trial setting
  • CDISC standards knowledge and experience
  • Minimum of 2 years’ experience working within a clinical CRO environment
  • Experience of programming tables, listings and figures output
  • Ability to manipulate input data to produce analysis datasets
  • Great attention to detail
  • Experience with other programming languages such as R and Python

 

Would Like

  • A statistical background
  • A degree in Mathematics, Computer Science, Statistics, Life Sciences or similar area

experience with complex and challenging projects, enabling you to progress your career and personal development.

You will be a part of a diverse, dynamic and talented multinational team gaining exposure to high profile, global studies for multiple international pharmaceutical and biotech clients.

To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Ashley Clarke on +44 (0) 1273 952 363 and send your CV through using the apply button on this page.