Oncology Research Nurse / Study Coordinator
We are seeking a professional, motivated, and detail-oriented Registered Nurse to join our growing Clinical Research team. The successful candidate will play a key role in coordinating oncology clinical trials, ensuring regulatory compliance, supporting patient care, and contributing to the advancement of cancer treatment.
This position is ideal for a nurse with strong organizational skills, excellent patient communication abilities, and an interest in clinical research.
Key Responsibilities
- Coordinate and manage oncology clinical trials from study start-up through close-out.
- Identify, recruit, screen, consent, and schedule eligible patients according to study protocols.
- Conduct study-related patient visits and assessments within scope of practice.
- Ensure accurate and timely completion of study documentation, source documents, and case report forms.
- Maintain Investigator Site Files, regulatory documentation, and study records.
- Liaise with Principal Investigators, sponsors, Clinical Research Associates (CRAs), laboratories, and ethics committees.
- Monitor patient safety and promptly report adverse events and serious adverse events according to protocol requirements.
- Ensure compliance with Good Clinical Practice (GCP), protocol requirements, ethical guidelines, and regulatory standards.
- Assist with data collection, query resolution, and preparation for monitoring visits and audits.
- Support patient education and provide ongoing patient care throughout clinical trial participation.
Job Type: Full-time
Pay: From R30 000,00 per month
Application Question(s):
- Are you currently registered with the South African Nursing Council (SANC)?
Experience:
- Clinical research or healthcare administration: 2 years (Required)
Work Location: In person
