Senior Statistical Programmer

  • Salary: Up to 108 CHF per hour
  • REF Number: 00051330
  • Consultant: Jocelyn Blackham
  • Contact: 0041 (0) 800 106 106
  • Date Published: 04.08.2021
  • Closed Date: 27.10.2021
  • Sector:
  • Location: Pratteln,
  • Discipline:

CK Group are recruiting for a Senior Statistical Programmer to join a rapidly growing biopharmaceutical company at their site based just outside of Basel on a contract basis.

Senior Statistical Programmer Role: The main purpose of the role will be to:

  • Implement and usage of programs to effectively analyse and report clinical trial data as the trial lead programmer.
  • Review trial documentation and provide feedback from statistical programming perspective, as well as study set-up in the reporting environment.
  • Play a key role in the definition of project and trial analysis data sets and metadata.
  • Work with lead statistical programmer and/or statistician, designs and implements trial and project analysis data sets and metadata including complex data derivations, data mapping and data pooling.

Further responsibilities will include:

  • Developing programs and generating tables, listings and figures for trial or project specific reports and statistical analyses in agreementwith trial documentation and guidelines from the principal statistical programmer and/or the statistician.
  • Performing and documenting quality control (QC) activities as per company standard operating procedures (SOPs), working practices, and guidance from the lead statistical programmer.
  • Managing critical issues within the project by pro-actively suggesting solutions to the lead statistical programmer and/or statistician.

Your Background: In order to be considered for this role, you will be required to have the following qualifications, skills and experience:

  • University degree (or equivalent) preferably in Mathematics, Informatics or other scientific discipline.
  • Advanced knowledge of programming in SAS and of statistical analyses in clinical trials.
  • Previous experience in statistical programming within a pharmaceutical company or a clinical research organization (CRO).
  • Previous experience in the review of Statistical Analysis Plans, study set-up and review of study specific documents, e.g. Clinical Protocol, CRF, annotated CRF, data validation guidelines.

This is an excellent opportunity to join a growing biopharmaceutical company based at their site in Allschwil.

Apply: For more information or to apply for this Senior Statistical Programmer position, please contact Jocelyn Blackham on 0041 (0) 800 106 106 or email jblackham@ckqls.ch, quoting job ref 51330.

Please could you send any correspondence in English.

It is essential that applicantshold entitlement to work in Switzerland.

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