Clinical Study Manager EMEA
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 and Medical Devices organization, based in Noord-Holland Netherlands.
Our Client focusses on the innovation of orthopaedic solutions
ROLE DESCRIPTION
As Clinical Study manager your main responsibility will be the operational support of all ongoing EMEA Clinical Studies. Including designing an start-up of the clinical studies, interaction with vendors and potential sites for nominations, qualifications but also the openings and the close-out of sites. Furthermore you are providing vendor management, budget oversight and ensure compliancy of the Investigator sites to the regulations and applicable laws.
RESPONSIBILITIES
You will take care of all clinical trials from start until the end. You will set up timelines, take care of budgets and set up operation plans. You take care of cross functional relations within the company and outside.
REQUIREMENTS
- Bsc, Msc or Phd in Biology, Medical, or Biomedical Engineering or other relevant Health-related fields
- At least 5 years of experience, and a minimum of 1 years as a Clinical study manager
- Fluent in English, additional european languages are a plus
- Good knowledge and understanding of ICH-GCP / ISO14155 and the applicable Medical Device regulations
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.
