Description
We are looking for a
Senior Programmer (m/f)
Reference: -en
Start: 11/16
Duration: 12 MM+
Place: in the Basel region
Branch: Herstellung von pharmazeutischen Spezialitäten und sonstigen pharmazeutischen Erzeugnissen
Your tasks:
- Responsible for the integrity of the programming/computing solutions for multiple clinical trials
- Act as scientific lead for programming expertise liaising with Biometrician and statistical scientific counterparts within the team, across multiple clinical trials
- Lead the full execution of final production output generation (tables, listings and graphics) for clinical trials
- In cooperation with the Biometrician/Statistical Scientist, develop study-level programming standards and ensure compliance with project-level/company standards
- Ensure high quality for all deliverables and follow the processes
- Ensure that documents and specifications are consistent and comply with company standards by providing input into eCRF and data structures, tables, listings and figures for Phase I-IV clinical trials and submission activities
Your qualifications
- Intermediate knowledge of/experience with SAS and other relevant programming software
- Working knowledge of database design/structures and basic statistics
- Good understanding of global clinical trial practices, procedures, methodologies
- Good understanding of regulatory requirements relevant for statistical programming (e.g. GCP, ICH)
- A profound work experience in a programming role, preferably supporting clinical trials/or in the pharmaceutical industry
Skills:
- Software developer