Clinical Research Coordinator
10AI EXPOSURE TODAY10
20-YEAR SCENARIO
NOT A FORECAST50%
NOT A FORECAST50%
THE DOOR · ENTRY DIFFICULTY TODAYB
STARTING PAY£24,000 - £29,000
REGULATORY MOATThe law requires human oversight. That human could be you.
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CAREERMASH (EN-ZA)FROM SUBJECTS ALLIED TO MEDICINE →
Clinical Research Coordinator
In South Africa, Clinical Research Coordinators (CRCs) are integral to the clinical trial process, ensuring that studies are conducted ethically and efficiently. As a CRC, you will manage the logistics of clinical trials, from participant recruitment to data management, while adhering to strict guidelines set by the South African Health Products Regulatory Authority (SAHPRA). This role is ideal for those who are organised and passionate about advancing medical science.
THE DOOR: ENTRY DIFFICULTY TODAY, graded A (easy) to E (extremely hard). A Careermash rule-of-thumb index built from our AI exposure index and the job's moat class. It is not a forecast and not a count of job openings.
AI EXPOSURE TODAY is a Careermash index from 0 to 100 of how exposed this job's everyday tasks are to AI today. We estimate it by matching published research on how people use AI to this job, usually by keyword or subject area, and we lower it where the work is protected (for example by physical, personal or legal requirements). It is not a direct measurement of how much people in this job use AI.
This job holds up well against AI
AI exposure today is low on our index (10), and the law requires human oversight. That human could be you. That is about as safe as careers get right now, though it is still worth learning to use the tools well.
The role
As a Clinical Research Coordinator in South Africa, you will oversee the planning and execution of clinical trials, ensuring compliance with SAHPRA regulations and ethical standards. Your role will involve recruiting participants, managing trial protocols, and collaborating with healthcare professionals. Strong organisational skills and attention to detail are crucial, as you will be responsible for maintaining accurate records and ensuring participant safety throughout the study.
Daily responsibilities
- Recruit and screen participants for clinical trials.
- Ensure compliance with SAHPRA regulations.
- Manage trial documentation and data collection.
Does a degree help here?
A UK degree in a relevant field is highly regarded in South Africa, as it demonstrates a strong understanding of research methodologies and ethical considerations. Employers often prefer UK graduates for their rigorous training and international perspective.