Job Descriptions
Thanks to our long experience in Belgium’s medical research sector and extensive contacts throughout this industry, our young consultant candidates are in a privileged position when it comes to the range and quality of jobs available.
The selection of interesting and rewarding jobs we offer changes all the time. So be sure to come back regularly to see what’s new for a full update.
Job details
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Clinical Data Managers
All collected data pass through the hands of the Clinical Data Manager. The CDM centralizes, verifies and validates this information in the clinical database and passes it on for further statistical processing. A job that requires great accuracy and precision.
Clinical Project Managers
The CPM coordinates all activities related to the clinical studies, such as follow-up and elaboration of the studies, budget monitoring, pharmacovigilance and data processing.
Clinical Research Associates
The CRA coaches the investigator and ensures that the study is conducted according to the applicable guidelines. He or she monitors the information in the patients' files and in the medical records. The CRA informs the investigator of possible erroneous and/or missing information and has it corrected or completed. A job with responsibility and content.
Clinical Research Physicians
The medical and clinical responsibility for the execution of the clinical studies lies in the hands of the CRP, who heads the project teams that work under his or her guidance.
Clinical Trial Assistants
The CTA is part of the project team and offers in-house support to the Project Manager and CRAs. The CTA has important administrative responsibilities. He or she also takes care of correspondence, filing and archiving, and additional tasks assigned within the clinical project.
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