About the Role
We are seeking an experienced and detail-oriented
Biostatistician
to join our clinical development team. In this role, you will be responsible for all biostatistical aspects of assigned clinical trials and projects, contributing to the design, analysis, and interpretation of clinical data to support regulatory submissions and scientific publications.
Key Responsibilities
* Lead biostatistical activities for assigned clinical trials and projects
* Provide expert input into trial design, objectives, and statistical methodologies
* Author statistical sections of clinical trial protocols, including sample size calculations
* Define randomization methods and strategies for handling missing data
* Develop and maintain statistical analysis plans (SAPs)
* Ensure compliance with SOPs, regulatory standards, and timelines
* Oversee statistical tasks outsourced to external service providers
* Present clinical trial results and contribute to clinical study reports
* Document statistical activities at study closure
Candidate Requirements
* University degree in statistics, mathematics, or a related discipline
* Minimum 5 years of experience as a statistician in clinical development (pharma, CRO, or academic research)
* Strong expertise in statistical methods applied to clinical trials
* Proven experience managing external service providers
* Knowledge of international clinical research regulations and GCP standards
* Proficiency in statistical software (SAS required; R preferred)
* Excellent interpersonal and communication skills
* Fluent in English (written and spoken)
Work Location:
Allschwil
Country:
Switzerland
Schedule:
Fulltime
Job Type:
12 month contract
*While we appreciate every application, please note that due to the high volume of responses, we may only be able to contact shortlisted candidates.
**Please note that we can only consider EU/Schengen applications