Senior Programmer (m/f)

REFERENZNUMMER:

319815/11

IHRE AUFGABEN:

-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

IHRE QUALIFIKATIONEN:

-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

WEITERE QUALIFIKATIONEN:

Software developer