Clinical Study Manager
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 Clinical Research organization, based in Netherlands.
Its foundations lie in specialized health research.
ROLE DESCRIPTION
In this role you are responsible for the clinical operations management and the total study overview
RESPONSIBILITIES
- Check and update reporting of resources, budget, timelines
- Estimate the feasibility of operational studies
- Decide on location, country, personnel
- Organize EC submissions
- Management of CRO and monitoring activities
- Review of clinical trial data and support preparation of clinical study reports
- Development of credible relationships
REQUIREMENTS
- MSc in life science or related field
- At least 3 years of experience in clinical research management
- Team player with strong interpersonal and communication skills
- Pro-active, dynamic and problem solving
- Good knowledge of GCP - ICH
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Hanneke de Koning.
