Clinical Research Nurse II – Flexible Day Hours

About the role

We are seeking a Clinical Research Nurse II to support multiple ongoing clinical trials. The position offers flexible day hours, up to 20 hours per week, and involves direct patient care, data collection, and coordination with study sponsors.

Key responsibilities

• Conduct clinical studies in accordance with FDA, GCP, and ICH regulations.
• Provide medical care and ensure patient safety throughout study visits.
• Schedule subject visits, obtain informed consent, and perform protocol procedures such as vital signs, ECGs, pregnancy tests, and blood sampling.
• Document all patient information, study data, and adverse events on required forms and electronic systems.
• Maintain IRB approvals, monitor compliance, and report any non‑compliance.
• Serve as primary sponsor contact, attend site initiation meetings, and communicate study status to stakeholders.
• Train and guide junior team members and act as backup to the direct manager.

Required profile

• Registered Nurse with experience in clinical research or trial coordination.
• Ability to work in an environment requiring PPE and handling hazardous materials.
• Strong organizational skills to manage multiple studies simultaneously.
• Excellent communication skills for interacting with participants, monitors, and internal teams.

Required skills

• FDA/GCP and ICH regulatory compliance.
• IRB submission and maintenance.
• Clinical assessments including vital signs, ECG operation, and blood sample collection.
• Adverse event identification and reporting.
• Study documentation and data entry accuracy.

What we offer

• Flexible day‑time schedule with a maximum of 20 hours per week.
• Opportunity to lead specific studies and train junior staff.
• Experience working with a multidisciplinary research team in a clinical setting.