CRA Medical Devices
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Limburg Belgium.
The company is a clinical research organisation is active in class II and III devices for therapeutic areas such as cardiology, anaesthesiology, plastic surgery and (endo-) vascular surgery.
ROLE DESCRIPTION
This CRA position is partially homebased, full time and on a permanent basis. Freelance is possible but definitely not preferred. Monitoring experience in the field of medical devices is requested.
RESPONSIBILITIES
Monitor study sites according to protocol ICH guidelines, GCP and SOP's. You report to the Senior CRA.
REQUIREMENTS
- A BSc/MSc in life sciences or a degree in a medical field
- 2-5 years of clinical monitoring experience, preferred in the field of medical devices
- Able to independently monitor study sites
- Fluent in English and Dutch; French is a plus
- Understanding of serious adverse event
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
