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 Noord-Brabant Netherlands. The company is a clinical development company.
Role descriptionAs a CRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. The position is on permanent basis and home-based.
Responsibilities- Monitor clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- All aspects of site management as prescribed in the project plans
- Negotiation of study budgets with potential investigators
Requirements- University degree in Life Science related field or degree as research nurse
- 2+ years of experience in clinical research
- Knowledge or experience with SOPs, ICH Guidelines and GCP
- Fluent in Dutch, French and English