Clinical Trials Coordinator
Location: BelgiumSIRE 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 Belgium.
The client is a pharmaceutical SME located in the Brussels area. They are involved in research and development of innovative technologies and galenic formulations
ROLE DESCRIPTION
The client is looking for a clinical trials coordinator to join its Clinical Department who will manage national and international clinical studies from phase I to phase IV
RESPONSIBILITIES
- Develop protocol and all other ICH documents
- Take part in study submission process to Regulatory Authorities
- Perform monitoring from initiation to close-out cisitis
- Coordinate study logistics with the manufacturing department
- Coordinate with CRO to assure respect of SOP's and GCP's
REQUIREMENTS
- University degree in medical, pharmaceutical or sciences
- Proven experience in phase I
- Knowledge of ICH and GCP
- English working proficiency
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
