Biostatistican (m/w)

Aufgaben:

- In general, work closely together with and support the Project Statistician (PSTAT) in submission related work. Collaborate     with other statisticians who are working at the trial and submission preparation level.
- Suggest and specify statistical analyses and review documents and output.
- Collaborate with Lead Programmer
- Specify and program inferential statistical analysis in SAS.
- Act as a fully responsible Trial Statistician for Phase 3 trials.

Skills:

- MSc/PhD in Statistics or Maths
- At least 4 years experience in international clinical development of Phase 3 studies and experience in submissions.
- Experience with studies in oncology
- Excellent statistical-methodological knowledge including an excellent working knowledge of SAS. Very good communication  

skills.

Required language skills:
- Fluent English. Knowledge of German would be an advantage, but is not required.

If you are interested in working in a challenging and exciting pharmaceutical environment in the South of Germany, this is an excellent opportunity. To find out more about the role, please send us your application via Email, stating the reference number.