You are an accurate and structured professional with a strong sense of responsibility. You understand the importance of reliable research data and handle confidential patient information with care. You can effectively manage deadlines, shifting priorities, and multiple projects simultaneously.

You take initiative, think ahead, and identify potential bottlenecks before they cause problems. Thanks to your analytical skills, you can critically assess medical information. You work independently but actively seek collaboration with colleagues and other stakeholders when necessary.

In addition, you recognize yourself in the following profile:

• You possess at least a higher professional education (HBO) working and/or thinking level, preferably with a completed (para)medical, biological, or other relevant education, or demonstrable experience in clinical research.
• You hold a current Good Clinical Practice certificate (GCP-WMO), or are willing to obtain one in the short term.
• You have an affinity for clinical scientific research. Experience with data management and tumor response criteria (such as RECIST) is a plus. You are willing to further develop your medical knowledge.
• You are digitally skilled and work easily with various databases and electronic registration systems.