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 Medical Devices organization, based in Noord-Brabant Netherlands. My client is a large international Medical Devices company.
Role descriptionYou will work at the department of digital pathology where you will contribute to clinical study design. this position is freelance, full time, on site and occasionally at a CRO, for at least one year.
ResponsibilitiesYou perform in house and aim for high quality statistical analysis. You co-write clinical study reports, support data management and develop study standards for internal and regulatory guidelines. You keep track of project analysis and associated documentation.
Requirements- Experienced in SAS, R experience is a plus
- Knowledge of GCP, ICH
- FDA and PMA experience
- Minimum 4 years in the clinical or pharmaceutical industry