Clinical studies 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 Healthcare and Pharmaceutical organization, based in Netherlands.
The company is a research center that focuses on nutrition and is located in a state of the art Life Science research center.
ROLE DESCRIPTION
The clinical studies manager will take care of the operational management of the clinical studies. This includes preparation, initiation, conduct, progress reporting and closure of the studies.
RESPONSIBILITIES
- Ensure progress reporting
- Assess operational feasibility of study
- develop study document, set-up and maintain study files
- Supervise third parties
- Safety reporting
- ...
REQUIREMENTS
- At least 4 years of experience in (international) clinical study management.
- Experience with Ethical Committee submission
- Knowledge of ICH-GCP guidelines
- Excellent communication skills, Dutch and English
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.
