Oncology Clinical Trial Coordinator

An Oncology Practice in the Western Cape is looking for an experienced Clinical Trial Coordinator. This is a 5/8 th position. The successful candidate will be responsible for providing expertise in the implementation, management, and evaluation of study protocols and research tools, supporting the development of new funding proposals, analysing qualitative / quantitative data and reports. Qualifications: Nursing or other relevant qualification. 2 years experience in a similar role. Key Duties: Conduct and facilitate start-up activities such as feasibility, site identification, pre-qualification, Site regulatory package review and approval, Clinical site agreements, Informed Consent , application, preparation, and submission, in accordance with relevant regulations, SOPs, and study-specific procedures. Client oriented. Screenings of Study Feasibilities. Enrolment Visits. Patient Eligibility. Computer literacy including MS-Office e.g. Excel and Word. Site Initiation visits. Interact professionally with external customers. Superior ability to manage multiple tasks with enthusiasm. Informed Consent discussions with patients. Screening visits. Treatment visits. Follow-up visits. Planning and coordinating pathology tests, radiology scans, and other results. Adverse Events, serious adverse events, and concomitant Medication. Closing date: 13 th March 2026 Requirements: Relevant tertiary qualification Drivers licence with own vehicle Qualifications: Nursing or other relevant qualification 2 years experience in a similar role