Beschreibung
Principal Programmer
Reference #:
8753SM
Location:
Basel (Switzerland)
Start:
ASAP
Duration:
6 months
Role:
The Principal Programmer is responsible for all programming aspects (including analysis datasets, pooled datasets, listings, figures, and tables) of individual Phase I-IV clinical trials and project-level activities for a drug project, provide technical expertise to offer consulting, training and mentoring other programmers and supporting operational excellence by working together with the statistical scientist and the biometrician.
Required Skills:
- Advanced knowledge of/experience with SAS and other relevant programming software.
- Proven experience in development of advanced MACROs with high programming efficiency; strong programming and problem-solving skills
- Proven experience in leading programmer support for multiple clinical trials and submission activities (or equivalent)
- Working knowledge of database design/structure and basic statistics. Working experience in pooling analysis datasets across multiple clinical studies (or equivalent)
- Good understanding of global clinical trial/project practices, procedures, methodologies.
- Good understanding of regulatory requirements relevant to statistical programming (eg GCP, ICH).
- Intermediate knowledge of office tools.
- At least 8 years work experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (5 years for MS Statistics/Computer Science graduates).
Education:
BA/BS/MS equivalent experience in mathematics, statistics, computer science, or health sciences/related field.
Languages:
Fluent English (oral and written)