You will be responsible for designing statistical methodologies and carrying out data analyses on preclinical, clinical and epidemiological studies in the framework of our clinical trial support services. Your mission: to integrate statistical principles and methodologies in the different phases of the clinical trials, using good statistical practices.

You will participate in the drafting of the statistical parts of the protocol, of the study reports and articles and draw up the statistical analysis plan. You will validate the reporting programs, the deliverables and schedule additional analyses when required.
Your experience and expert knowledge of SAS software will enable you to interpret and analyze the results.

You have a graduate degree in statistics and 2 to 5 years of experience in a similar position in a pharmaceutical laboratory or CRO.
You have perfect command of SAS software. You are thorough and organized, and have a good knowledge of the different types of analyses as well as excellent communication skills enabling you to work effectively with multidisciplinary teams.