Biostatistician – Clinical Trials

For our client, a leading pharmaceutical company based in Switzerland, we are looking for a

Biostatistician – Clinical Trials 80% - 100% (Ref. Nr. 3006)
Phase I-III studies – innovative therapies

Your main tasks

• Design and develop statistical analysis plans (SAPs) for clinical trials across all phases.

• Perform statistical analyses using SAS and R, and generate tables, listings, and figures (TLFs).

• Collaborate with clinical teams on study design, sample size estimation, and endpoint selection.

• Review clinical study reports (CSRs) and contribute to regulatory submission documents.

• Provide statistical expertise for Data Safety Monitoring Board (DSMB) meetings.

Your profile

• Master's or PhD in Biostatistics, Statistics, or Mathematics.

• 3-6 years of experience in pharmaceutical biostatistics or CRO environment.

• Proficiency in SAS (Base, STAT, Graph) and R programming.

• Knowledge of CDISC standards (SDTM, ADaM) and ICH E9 guidelines.

• Strong analytical thinking and ability to communicate complex results clearly.