Perform quality control and validation checks to ensure consistency and quality of clinical data and trial outputs; Program SAS macros to analyse and report clinical trials and the associated research projects (e.g. translational research, quality of life, etc.); Program trial-specific data listings and reports (e.g. for data management or medical reviews); Provide special reports, data listings or graphs upon request; Provide programming support and advice to biostatisticians within the Statistics team and other functions within SAKK; Participate in unit and cross-functional activities aimed at optimizing and standardizing processes
Requirements:
Bachelor’s Degree or Master’s Degree/Diploma in medical documentation, computer science, statistics or related field with at least 3 years’ experience as programmer; experience in clinical trials and in oncology would be advantageous Proficient in SAS Strong problem solving skills and ability to work both independently and in teams Very good project management skills Excellent written and oral communication skills in English; ability to communicate in German
