Clinical Research Nurse

What You’ll Be Responsible For: Managing and overseeing multiple clinical studies involving both patients and healthy volunteers with precision and care. Maintaining comprehensive and accurate study documentation that complies with protocol and regulatory guidelines. Providing exceptional medical oversight, prioritizing participant safety throughout all trial activities. Scheduling participant visits, managing recruitment efforts, and supporting ongoing engagement to optimize retention. Executing protocol-specific procedures such as informed consent, vital sign assessments, pregnancy screenings, ECGs, and more. Ensuring source data accuracy, updating participant files, and correctly recording data into electronic systems. Collaborating on ethics submissions and ensuring compliance with all ethical and safety standards. Participating in site initiation, training sessions, and team meetings to ensure seamless trial execution. Providing clear communication with participants through follow-up calls, appointment reminders, and information dissemination. Assisting with maintaining the cleanliness and organization of the clinical environment and proper waste disposal protocols.

What You Bring to the Role: A bachelor’s degree or equivalent in a healthcare or medical discipline. Valid nursing registration issued by the Dutch healthcare authority. At least 2 years of relevant experience in clinical care or research settings. Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, Standard Operating Procedures (SOPs), and clinical trial processes. Exceptional attention to detail, analytical skills, and the ability to work independently. Excellent communication skills; fluency in English is a plus. Proficiency in basic computer applications and documentation management. Organizational prowess with the ability to prioritize multiple tasks efficiently. Discretion, professionalism, and good judgment in handling sensitive information.

Nice to Have: Experience working in hospital or dedicated research settings. Familiarity with electronic data capture (EDC) systems. Multidisciplinary team collaboration experience. Additional languages relevant to multicultural participant groups. Preferred Educational & Professional Background: Formal healthcare qualifications with proven research experience. Previous work experience within the Netherlands clinical research landscape is advantageous.

Additional Details: This position is based fully onsite in Utrecht; candidates residing locally preferred Commitment to safety protocols, maintaining a professional environment, and ensuring the highest standards of participant care.

Ready to make a meaningful impact in clinical research? If you’re driven, detail-oriented, and eager to contribute to pioneering studies, we look forward to receiving your application. Take the step towards your next rewarding career opportunity today!