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-US)FROM SUBJECTS ALLIED TO MEDICINE →
Clinical Research Coordinator
As a Clinical Research Coordinator (CRC) in the United States, you play a pivotal role in the healthcare landscape, managing clinical trials that test new medications and therapies. This position is not just about paperwork; it's about ensuring patient safety and data integrity while working closely with medical professionals and researchers. The CRC is the backbone of clinical research, making it an exciting and rewarding career for those passionate about medicine and innovation.
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
In the US, Clinical Research Coordinators are responsible for overseeing the day-to-day operations of clinical trials. This includes recruiting and screening participants, ensuring compliance with regulatory requirements, and managing study documentation. CRCs act as a liaison between the research team and participants, making communication skills essential. You will also be involved in data collection and analysis, contributing to the advancement of medical science.
Daily responsibilities
- Recruit and screen participants for clinical trials.
- Ensure compliance with regulatory and ethical standards.
- Manage study documentation and data collection.
Does a degree help here?
A UK degree in a relevant field provides a strong foundation in research methodologies and ethics, giving you a competitive edge in the US job market. UK graduates are often viewed as having a rigorous academic background, which is highly regarded by employers in the clinical research sector.