An academic medical center is looking for an enthusiastic monitor to strengthen its monitor unit. As a monitor, you contribute to safeguarding and improving the quality with which studies by researchers are conducted in participating hospitals. This concerns Investigator Initiated studies in phase I, II, and III, within a diversity of disease profiles and specialisms. You will be part of an ambitious and growing team.
What you will do.
- Visit hospitals in the Netherlands and, to a limited extent, Belgium.
- Advise researchers on setting up monitoring for their own study.
- Draw up monitoring plans.
- Be involved in the preparation of various hospital visits.
- Conduct study-specific visits, initiation visits, and close-out visits.
- Report findings and advice in monitoring reports.
- Guide researchers in resolving identified findings.
- The role is comparable to that of a Clinical Research Associate (CRA).
Profile
- Relevant work experience.
- Show initiative, have organizational talent, work carefully, and want to develop in the field of clinical studies.
- Proactive mentality.
- HBO or academic level education with the necessary (bio)medical knowledge and scientific skills.
- Good command of reading and writing Dutch (strict requirement).
- Driving license and access to a car, and willing to travel regularly.
- Strong communicator, show courage, and dare to discuss issues.
- Contributing to the optimization of work processes is self-evident for you.
- Knowledge of regulations concerning clinical research (a plus).
- Work experience with clinical (drug) research, preferably in a role as monitor/CRA, data manager, research coordinator, as a PhD student, or similar (a plus).
- Able to provide a recent GCP or BROK certificate (a plus).
- Providing a Certificate of Conduct (VOG), a valid identity document, and relevant diplomas is a condition for appointment.
How to apply
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