Biostatistician
Location: NetherlandsSIRE 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 Noord-Brabant Netherlands.
The client is delivering innovative solutions to make sure that healthcare specialist can search more efficient for patient specific treatment, and therefore treat patients in the best way possible.
ROLE DESCRIPTION
You 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.
RESPONSIBILITIES
- Ensure high quality and correct statistical analyses, performed in-house or with a CRO
- Contribute to clinical study design,
- Able to work with data from different sources
- Develop and comply with project / study standards and specifications following internal and regulatory guidelines
- Managing statistical programming activities
REQUIREMENTS
- Bachelor or Master in Biostatistician or Bioinformatics
- Excellent communication skills ins English
- 5+ years' working experience with SAS, knowledge of R is a plus
- 4+ years' of experience in a pharmaceutical or clinical divide industry
- Understanding of regulatory requirements (e.g., GCP, ICH) and clinical data presentation standards
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Mirte van Hal.
