Senior Statistical Programmer

☞ PharmiWeb.Jobs

View: 177

Update day: 25-04-2024

Location: Allschwil Basel-Landschaft BL

Category: R & D IT - Software

Industry: Staffing Recruiting

Position: Associate

Job type: Contract

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The Life Science Career Network CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

SENIOR STATISTICAL PROGRAMMER– 4778

Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a Senior Statistical Programmer for a contract based in Basel area.

The ideal candidate should have atleast 5 years of years of experience in SAS Programming and statistical analysis in Clinical trials

Main Responsibilities
  • Responsible for the implementation and use of programs to effectively analyze and report clinical trial data as the trial lead programmer
  • Responsible for the review of trial documentation and providing feedback from statistical programming perspective, as well as study set-up in the reporting environment
  • Responsible for the definition of project and trial analysis data sets and metadata
  • In agreement with the 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
  • Manage critical issues within the project by pro-actively suggesting solutions to the lead statistical programmer and/or statistician
  • Develops programs and generates tables, listings and figures for trial or project specific reports and statistical analyses in agreement with trial documentation and guidelines from the principal statistical programmer and/or the statistician
  • Performs and documents quality control (QC) activities as per Companies standard operating procedures (SOPs), working practices, and guidance from the lead statistical programmer
Qualifications And Experience
  • Relevant working/residency permit or Swiss/EU-Citizenship required.
  • 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
  • Min of 5 years’ experience in statistical programming within a pharmaceutical company or a clinical research organization
  • 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
  • Knowledge of all aspects of clinical trials from initial study set-up to study completion with an excellent understanding of the roles and responsibilities of all related disciplines, e.g. Biostatistics and Clinical Data Management
  • Good knowledge and understanding of CDISC, especially SDTM and ADaM
  • Basic knowledge of R, knowledge of other programming languages and of data management principles and tools is an asset
  • Proven record to work independently, analyze problems and formulate ideas in a structured and logical manner
  • Knowledge of international clinical research regulations and requirements (ICH-GCP)
  • Excellent interpersonal and communication skills
  • Fluent in English (written and spoken)
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Deadline: 09-06-2024

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