Distribution across 35 profiles.
Middle half of Clinical Research Coordinators score between 29% and 36%.
0%
50%
100%
p10 · 26%
39% · p90
Task breakdown by work type
On-screen work40%
Done entirely on a computer. High AI exposure — these tasks are already in the automation zone.
In-person + screen44%
Physical sensing, digital output — e.g. interviewing someone then writing a report. Partially protected.
Computer + action0%
Computer input, real-world output — needs someone to act on it, not just software.
Fully in-person16%
No computer required. Furthest from automation — the strongest human advantage.
Typical tasks
3 synthetic profiles for a Clinical Research Coordinator, ordered by automation exposure.
Tab between them to see how task mix drives the score difference.
TaskTimeTypeExposure
Recruiting and screening study participants by reviewing medical records, conducting phone interviews, and explaining study details to potential candidates
deep expertisesocial core
25%AD
7%
Collecting, processing, and managing study data, including entering information into electronic data capture (EDC) systems, verifying accuracy, and resolving discrepancies
23%DD
60%
Ensuring compliance with study protocols, regulatory requirements, and ethical guidelines by maintaining documentation, submitting reports to institutional review boards (IRBs), and preparing for audits
14%DD
62%
Coordinating study visits, including scheduling appointments, arranging transportation or lodging for participants, and ensuring all necessary tests and procedures are completed on time
11%AD
21%
Communicating with study sponsors, principal investigators, and other team members to provide updates, report adverse events, and address any issues that arise during the study
deep expertisesocial core
9%AD
10%
Administering study interventions (e.g., dispensing investigational drugs, performing minor procedures like blood draws or ECGs) under the supervision of a principal investigator
deep expertisesocial core
8%AA
6%
Training and supervising junior staff or volunteers involved in the study, including explaining protocols, demonstrating procedures, and ensuring adherence to guidelines
deep expertisesocial core
7%AA
1%
TaskTimeTypeExposure
Collecting, processing, and managing study data, including entering information into electronic data capture (EDC) systems, verifying accuracy, and resolving discrepancies
23%DD
52%
Ensuring compliance with study protocols, regulatory requirements, and ethical guidelines by maintaining documentation, submitting reports to institutional review boards (IRBs), and preparing for audits
20%DD
63%
Coordinating study visits, including scheduling appointments, arranging transportation or lodging for participants, and ensuring all necessary tests and procedures are completed on time
16%AD
22%
Communicating with study sponsors, principal investigators, and other team members to provide updates, report adverse events, and address any issues that arise during the study
deep expertisesocial element
16%AD
13%
Administering study interventions (e.g., dispensing investigational drugs, performing minor procedures like blood draws or ECGs) under the supervision of a principal investigator
deep expertisesocial core
9%AA
0%
Recruiting and screening study participants by reviewing medical records, conducting phone interviews, and explaining study details to potential candidates
9%AD
32%
Training and supervising junior staff or volunteers involved in the study, including explaining protocols, demonstrating procedures, and ensuring adherence to guidelines
deep expertisesocial core
4%AA
1%
TaskTimeTypeExposure
Collecting, processing, and managing study data, including entering information into electronic data capture (EDC) systems, verifying accuracy, and resolving discrepancies
42%DD
68%
Administering study interventions (e.g., dispensing investigational drugs, performing minor procedures like blood draws or ECGs) under the supervision of a principal investigator
deep expertisesocial core
16%AA
0%
Ensuring compliance with study protocols, regulatory requirements, and ethical guidelines by maintaining documentation, submitting reports to institutional review boards (IRBs), and preparing for audits
15%DD
48%
Recruiting and screening study participants by reviewing medical records, conducting phone interviews, and explaining study details to potential candidates
deep expertisesocial core
12%AD
12%
Training and supervising junior staff or volunteers involved in the study, including explaining protocols, demonstrating procedures, and ensuring adherence to guidelines
deep expertisesocial core
7%AA
7%
Coordinating study visits, including scheduling appointments, arranging transportation or lodging for participants, and ensuring all necessary tests and procedures are completed on time
4%AD
26%
Communicating with study sponsors, principal investigators, and other team members to provide updates, report adverse events, and address any issues that arise during the study
deep expertisesocial core
1%AD
9%
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AI tools for this role
Tools relevant to the most automatable tasks in this profession.
