CRO Antwerp
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 Clinical Research organization, based in Belgium.
It's a very small company with only 14 employees. They are based in Antwerp and work according to projects. Specialised in implanon they focus on birth control studies since 2000. It's a cosy and informal company very close located to the station in lively Antwerp.
ROLE DESCRIPTION
You will be working in a team of 5 people and dependant on the length of the project there will be 5 more CRA's joining you. You'll monitor and accompany medical investigations from the farmaceutical industry and play a part in the performance and surveillance of the quality of the investigation.
It's a very educational and alternating job where you'll be tested on all of your abilities.
RESPONSIBILITIES
Your responsibilities will differ from time to time because you will probably will be working with a few CRA's in the same team but the main activities will exist of:
- Writing drug trial methodologies (procedures)
- Identifying and briefing appropriate trial investigators (clinicians)
- Setting up and disbanding trial study centres
- Designing trial materials and supplying study centres with sufficient quantities
- Providing clinicians with instructions on how to conduct the trials
- Collecting and authenticating data collection forms (commonly known as case report forms)
- Monitoring progress throughout the duration of the trial
- Writing reports
REQUIREMENTS
- MSc/Bsc or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
- Extensive clinical monitoring experience
- Extensive understanding of SOPs, WI, FDA, and local regulations as well as ICH GCP guidelines
- Effective command of written and spoken English language
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Romy van Ooijen.
