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 e...