Clinical trial assistent
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 Brabant Flamand Belgium.
This international organisation is specialised in developing, producing and selling of medicines
ROLE DESCRIPTION
You will be supporting the clinical study staff within the Clinical R&D, and will be responsible for tracking and filling of the Study documents and managing the clinical master files.
RESPONSIBILITIES
- According to regulations and guidelines track study documents and ensure for completeness of the Trial master file for clinical studies.
- Make sure the regulatory binders are created and distributed.
- Respond to issues regarding study files and assist on implementing corrective or preventive actions.
- Internal communications assistance regarding clinical data and events.
- Support of safety committee meetings, provide safety documentation to functional groups.
- Assist on logistics for investigator meetings and expert panel meetings .
- Distribution of newsletter assistance .
REQUIREMENTS
-A Bachelor Degree
- a minimum of 1 year experience in administrative support or equivalent
- experience with computer systems or MS Office programms
- organisational skills and attention to details
OTHER
Experience with clinical research or a background in clinical or medical is considered a plus
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.
