SIRE 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 companyOur client is a professional Clinical Research organization, based in Zuid-Holland Netherlands. The company is a CRO for pharmaceutical, biotechnology and medical devices companies
Role descriptionYou will act as a member of the clinical monitoring team with the responsibility that everything is compliant with study guidelines, SOPs etc.
Responsibilities- Perform site visits and monitor activities in accordance with protocol, GCP/ICH Guidelines, and other applicable regulatory requirements.
- Mentor CRAs.
- Evaluate overall performance of site and site staff .
- Maintain working knowledge of GCP/ICH Guidelines
Requirements- Bachelor degree in relevant field
- 2+ years of prior clinical monitoring experience
- GCP/ICH knowledge
- Excellent communication skills in Dutch and Englisch