CRA (Home based)
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 Pharmaceutical organization, based in Netherlands.
The client is a global CRO that operates in both the pharmaceutical and biotech industry.
ROLE DESCRIPTION
As 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. This CRA position is fully home-based, full time and on a permanent basis.
RESPONSIBILITIES
Monitor clinical study sites according to protocol ICH guidelines, GCP and SOP's
REQUIREMENTS
- A MSc in life sciences or a degree in a medical field
- 2-5 years of clinical monitoring experience in the field of oncology
- Able to independently monitor study sites
- Full Fluency in writing and speaking of English and Dutch
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Michael Kooiman.
