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