SIRE 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 companyOur client is a professional Clinical Research and Pharmaceutical organization, based in Netherlands. They are specialized in IBD research with offices all over the world. They have expertise in trial’s focused on Crohn’s disease and Ulcerative Colitis. Since 1986 they have collaborated with pharmaceutical and biotechnology industries, government agencies, and academic investigators in the performance of global, multi-centre, randomized controlled trials.
Role descriptionAs a Clinical Research Officer you will be responsible for administrative, clerical, implementation and processing to the project teams and stakeholders. You’ll coordinate meetings and act as first point of contact for project queries. You'll be working fulll-time on a project-based at the office in Amsterdam for at least one year with a chance on outflow. You will report to the project director.
ResponsibilitiesYou'll contribute to the creation and maintenance of project forms, assist the team, providing timely administrative support, including form preparation, client/project information entry, creating logs, reports, and scripts
- Project support
- Document management
- Client/sponsor support
- Document control
Requirements- BSc/ MSc
- +- 1-3 years of related work experience or a minimum of one-year College Advance Degree in Life Sciences/Health or Clinical Research.
- Ability to work in a cross-functional environment
- Available for at least 1 year
- Fluent in Dutch