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 client is a subsidiary of a global pharmaceutical company.
Role descriptionAs the clinical registry you are tasked with posting accurate and consistent info on up to 40 global registries. You support all companies in pharma, consumer and medical device operations with disclosure studies. You are positioned between clinical, medical, development, regulatory and local companies.
ResponsibilitiesYou provide knowledge on clinical registry and keep all requirements for regulatory disclosure documents in check. You get information and interpret all local disclosure requirements. You keep all registration and disclosure intel up to date.You are part of all clinical registry team projects and enhance processes.You are responsible for keeping balance of project team priorities.
Requirements- Bachelor degree in science
- Minimum of 5 years experience in industry R&D or Quality
- Experience in regulated medical industry
- Knowledge of (pre-) clinical drug development is a plus
- Strong leadership persona
- Fluent in English