As a Senior Biostatistician, you will be responsible for the development of statistical standards for clinical trials. You will write the statistical analysis plans and perform the statistical analyses for clinical trials.

Besides, you will act as a statistical adviser for the Biostatisticians and programmers in the assigned therapeutic areas. You will monitor the statistical and programming activities of the team. You will also be in charge of the statistical analysis and the statistical part of the report.

In addition, you will represent the company externally (conferences, contact with clients…)

We are looking for an experienced Biostatistician with at least 7years experience within a pharmaceutical company, a CRO or a biotechnology. You have an MSc or a PhD in Statistics or equivalent combined with excellent knowledge of SAS programming for clinical trials.

You are an excellent communicator and speak fluently English (Knowledge of German or French is an asset). You have experience in leading teams and resolving problems with a positive approach.

You also have a strong knowledge of regulatory guidelines specific to the pharmaceutical industry and clinical development.

The client is offering a permanent opportunity within an international environment with an excellent basic salary. In addition, there is a relocation package, bonus scheme and excellent benefits. You will be working in a multicultural environment and will benefit from the outstanding quality of life that Switzerland has to offer.

If this opportunity is matching your career prospect, send me your CV with a cover note by email or call Louise Beka to discuss this role and similar position in confidentiality.

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business