|Publication date:||November 25 2019|
|Function Group:||Clinical Research|
Our client is a leading and fast-growing organisation in the medical devices industry with a global presence. The company operates in more than 400 locations all over the world. They are performing multiple clinical studies worldwide and are located in Limburg, the Netherlands.
As a statistician you will report directly to the statistics manager and your responsibilities are all related to several subjects, such as: clinical trial protocols, evaluation of clinical studies, documentation of study results, regulatory submissions, and the presentation of study results.
In a cross-functional team you will manage several smaller and larger project simultaneously. You will work on study objectives to ensure safety and efficacy of the devices. Additionally, you will perform analyses of study data and documentation, you will perform justifications of methods, analyses and results throughout several types of reports, and you will identify potential threats to the credibility and validity of the study.
It is expected of you to stay up-to-date on all relevant statistical programs and perform statistical program development and validation. You will design case report forms and statistical analysis plans.
This growing and innovative organisation offers:
If you are interested in this job, or in similar ones, please feel free to contact me directly.
Consultant Quality & Clinical | Medical Devices