Clinical Research Coordinators
Management Occupations- Code O*NET-SOC
- 11-9121.01
Plan, direct, or coordinate clinical research projects. Direct the activities of workers engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives. May evaluate and analyze clinical data.
Les intitulés des métiers et les énoncés de tâches sont affichés en anglais, tels que publiés. Les libellés, y compris les types de tâches, sont traduits.
Exposition à l'IA
- Source des données: BLSPublié: 2026-08
Élevée· relative
FaibleQuatre bandes relativesTrès élevéeValeur par groupe professionnel
Échelle, base et source
Quatre bandes relatives (Faible / Modérée / Élevée / Très élevée)
831 métiers détaillés du tableau des projections d'emploi du BLS. La valeur est attribuée par code de la National Employment Matrix (NEM), si bien que les métiers partageant un code NEM reçoivent la même bande
- Source des données: AnthropicPublié: 2026-03
0.061
0.000Étendue des valeurs présentées ici0.745Valeur par groupe professionnel
Échelle, base et source
Indice d'exposition observée, 0–1 tel que publié
Rapporté aux tâches O*NET
Publié par profession SOC 2018 ; chaque profession O*NET ayant le même code SOC 2018 reçoit cette valeur
- Source des données: ILOPublié: 2025
0.40
0.09Étendue des valeurs présentées ici0.70Valeur par groupe professionnel
Échelle, base et source
Indice d'exposition à l'IA générative, 0–1 tel que publié
Publié par groupe de base ISCO-08. Relié à ce métier, en tout ou en partie, en appliquant tels que publiés les tableaux de correspondance du U.S. Bureau of Labor Statistics (ISCO-08 vers SOC 2010, SOC 2010 vers SOC 2018)
Quelle est la nature de la valeur publiée par cette source
La catégorie BLS est un rang relatif et non un niveau absolu, et ce n'est pas une mesure de première main : elle regroupe en quatre bandes les rangs centiles du métier dans plusieurs études publiées. Ce n'est ni une prévision d'emploi ou de salaire, ni une probabilité d'adoption, et elle ne distingue pas automatisation et augmentation.
Exposition à l’IA (grille d’OpenAI)
33 tâches évaluées · 30 tâches avec β ≥ 0,5 (90.9%)
β = exposition directe (E1) + 0,5 × exposition lorsque des outils sont disponibles (E2), selon la définition du dépôt source.
- Unité source : tâches O*NET 27.2 → code de métier O*NET 31.0
- Toutes les tâches notées figurent dans la liste des tâches O*NET 31.0.
- Source
- OpenAI "GPTs are GPTs" exposure rubric
- Version
- gh-main-0471612
- Licence
- MIT License, Copyright (c) 2024 OpenAI
Tâches
Énoncés de tâches de l’O*NET® 31.0 Database, les tâches principales d’abord.
| Tâche | Type | β (OpenAI) |
|---|---|---|
| Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. | Principale | 0,5 |
| Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. | Principale | 0,5 |
| Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms. | Principale | 0 |
| Develop advertising and other informational materials to be used in subject recruitment. | Principale | 1 |
| Confer with health care professionals to determine the best recruitment practices for studies. | Principale | 0,5 |
| Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts. | Principale | 0,5 |
| Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks. | Principale | 0,5 |
| Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies. | Principale | 0,5 |
| Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. | Principale | 1 |
| Participate in the development of study protocols including guidelines for administration or data collection procedures. | Principale | 0,5 |
| Oversee subject enrollment to ensure that informed consent is properly obtained and documented. | Principale | 0,5 |
| Order drugs or devices necessary for study completion. | Principale | 0,5 |
| Organize space for study equipment and supplies. | Principale | 0 |
| Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data. | Principale | 1 |
| Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures. | Principale | 0,5 |
| Inform patients or caregivers about study aspects and outcomes to be expected. | Principale | 0,5 |
| Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions. | Principale | 0,5 |
| Direct the requisition, collection, labeling, storage, or shipment of specimens. | Principale | 0 |
| Contact outside health care providers and communicate with subjects to obtain follow-up information. | Principale | 0,5 |
| Communicate with laboratories or investigators regarding laboratory findings. | Principale | 0,5 |
| Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. | Principale | 0,5 |
| Code, evaluate, or interpret collected study data. | Principale | 1 |
| Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses. | Principale | 0,5 |
| Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols. | Principale | 0,5 |
| Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. | Principale | 0,5 |
| Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms. | Principale | 0,5 |
| Solicit industry-sponsored trials through contacts and professional organizations. | Complémentaire | 0,5 |
| Register protocol patients with appropriate statistical centers as required. | Complémentaire | 1 |
| Participate in preparation and management of research budgets and monetary disbursements. | Complémentaire | 0,5 |
| Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics. | Complémentaire | 0,5 |
| Contact industry representatives to ensure equipment and software specifications necessary for successful study completion. | Complémentaire | 0,5 |
| Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary. | Complémentaire | 0,5 |
| Arrange for research study sites and determine staff or equipment availability. | Complémentaire | 0,5 |
Informations professionnelles
Sources et attribution
This page includes information from the O*NET® 31.0 Database (https://www.onetcenter.org/database.html) by the U.S. Department of Labor, Employment and Training Administration (USDOL/ETA). Used under the CC BY 4.0 license (https://creativecommons.org/licenses/by/4.0/). O*NET® is a trademark of USDOL/ETA. AI Changing Work has modified all or some of this information: the O*NET-SOC code, title and task statements are reproduced in English without change; task-type labels are shown in the page's language and tasks are listed core first; any Korean occupation title shown on the Korean-language page is AI Changing Work's translation; any KSCO-8 unit groups linked to this occupation were paired with it by AI Changing Work's judgment, and the relation labels and statuses are AI Changing Work's additions. USDOL/ETA has not approved, endorsed, or tested these modifications.
Any AI exposure figures on this page are published by third parties, not by AI Changing Work, and none is part of the O*NET information. OpenAI publishes task-level scores (MIT License) for O*NET 27.2 task statements; each is shown next to the O*NET 31.0 task statement with the same task ID, whose wording can differ from the 27.2 statement that was scored. OpenAI also publishes occupation-level scores for O*NET-SOC codes in the same release, and any such score is shown on the O*NET occupation with the same code. Anthropic publishes an observed exposure index in the Anthropic Economic Index (CC-BY), and the U.S. Bureau of Labor Statistics publishes relative AI exposure categories (public domain); both are published per SOC code, and each value is shown on every O*NET occupation with that code. The International Labour Organization publishes a generative AI exposure index in ILO Working Paper 140 (CC BY 4.0) for ISCO-08 unit groups; AI Changing Work links those groups to O*NET occupations by applying the U.S. Bureau of Labor Statistics ISCO-08 to 2010 SOC and 2010 SOC to 2018 SOC crosswalks as published, without case-by-case selection, and these crosswalks match many groups only in part. Where several unit groups are linked, each group's published value is listed, and any summary shows only the lowest and highest of those values with the number of groups; no exposure figure is averaged or recalculated. Any employment figures are published by the U.S. Bureau of Labor Statistics for the SOC group containing this occupation. Each source is credited where its figures are shown.
O*NET OnLine: 11-9121.01 Clinical Research Coordinators
KSCO 코드·명칭: 한국표준직업분류(제8차 개정) — 통계청 고시 제2024-328호 (2024-07-01 고시, 2025-01-01 시행). 저작권법 제7조 제2호의 고시 항목이다. 명칭 표기(가운뎃점·띄어쓰기)는 해설서 2차 정오 반영판의 표기를 따랐으며, 고시 항목표와는 18개 명칭에서 가운뎃점 글리프나 띄어쓰기만 다르다. 통계청은 2025년 10월 국가데이터처로 개편되었다. 이 페이지의 KSCO 연결은 통계청·국가데이터처의 공식 연계표가 아니다.