Job Description
As Biostatistical Analyst you will be responsible for:
1. Development of analysis datasets (CDISC ADaM format) via SAS programming
2. Development of analysis tables, listings and figures via SAS programming
3. Implementation of CDISC standards in clinical trials
4. Quality control of project deliverables
5. Creation of the Statistical Analysis Plan and mock TLFs for Phase I studies
6. Production and optimization of system tools and macros
Qualifications
What do you need to be successful?
7. Bachelor/Master in IT or master’s in sciences (biomedical, biology, pharmacy, …) with affinity for programming
8. Knowledge of SAS (BASE-STAT-GRAPH-macros-…) is a plus. Additional training can be provided
9. You have good communication skills
10. You have an excellent knowledge of English. Knowledge of Dutch is an asset
11. You are a well-organised colleague with an analytical mind
12. You’re eager to learn new things
13. You want to work in a young and dynamic group of clinical programmers and statisticians
14. Any relevant job experience is an asset