As a clinical research associate, you will be responsible for participating in trial setup activities.
The tasks include preparing and finalizing study documents, conducting site qualification visits, monitoring visits, and close-out visits at assigned clinical sites. You will also write site visit reports and manage IMP management processes.
You will work closely with other CRAs and the Study Team to ensure quality and milestones are achieved within the project scope.
Qualifications
* You have obtained a university degree in (para-) medical, pharmaceutical, sciences, life-sciences or biosciences. Relevant qualifications by experience may also be acceptable.
* You can work independently with a sense of urgency and limited need for oversight.
* You are fluent in English; knowledge of French is an asset.
* You are a strong communicator and have strong organizational skills.
* You work well independently as well as in a team.
* You are accountable, helpful, dedicated and flexible.
Besides these essential requirements, being able to travel is highly appreciated.
Benefits
* This role offers a unique opportunity to develop your skills in clinical research and contribute to the success of our projects.
Other Opportunities
* We offer training and professional development opportunities to help you achieve your goals.
Conclusion
If you want to take your career to the next level and become a valuable member of our team, please send us your story and resume via the apply button. We look forward to hearing from you!