You will inspire others and act as a role model for junior CRAs following our internal training program, guiding them through their professional development.
We value the personal development of our employees and encourage you to grow in your role, offering opportunities for further development beyond your core tasks.
We offer a contract for a minmal of 36 hours per week with the potential for a permanent position, along with the chance to assist in our internal training program for CRAs.
A completed university degree in Life Sciences or a similar field, with at least 2 years of experience as a CRA/Monitor in clinical studies.
A strong understanding of local and European laws, regulations in clinical research, and ICH-GCP guidelines, with a focus on accuracy.
Fluency in both Dutch and English, both spoken and written, along with a team-oriented mindset and the ability to work independently.
You are accurate and thorough in your work, ensuring compliance with all regulations and guidelines in clinical research.
You enjoy working independently, taking responsibility, and proactively solving problems as they arise.
You have a collaborative mindset, working effectively with colleagues while also being able to manage your individual tasks.
If you are living in the Netherlands and identify with the profile above or would like to learn more about the role, please contact us at: [email protected].
Acquisition in response to this vacancy is not appreciated.
