Clinical Trial Administrative Support
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 and Pharmaceutical organization, based in Brussel Belgium.
Specialised in the developing, producing and selling of medicines.
ROLE DESCRIPTION
Within the department you will be responsible for the support of the clinical staff, tracking and filling study documents and managing the trial master files.
RESPONSIBILITIES
- Assuring the compliancy of the ICH-GCP regulations, and completeness for the Trial master file
- React to study document related problems, and assist on implementation with corrective or preventive actions
- Internal communication voor assistance in clinical data and events
- Support the safety committee meetings , in delivery of safety documentation to functional groups
- Assisting on logistic processes for research and expert panel meetings.
REQUIREMENTS
- Bachelor or Masters degree in pharmaceutical sciences or related area's
- 1 year of experience with the Trial master file, and administrative experience.
- Experienced in Microsoft Office programs
- Detail orientated and organisational skills
- Fluent in English
OTHER
A minimum of 1 year experience with the trial master file and fluency in English is required
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.
