Clinical Research Coordinators

O*NET-SOC 代码: 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.

数据来源: BLS发布时间: 2026-08
高· 相对
低四级相对区间很高
职业群单位数值
尺度 · 母数 · 来源
四级相对类别（低 / 中等 / 高 / 很高）
以BLS就业预测表中831个细分职业为基数。取值按 NEM（全国就业矩阵）代码给定，因此共用同一 NEM 代码的职业得到相同分档
来源数据集（XLSX 文件下载）
数据来源: Anthropic发布时间: 2026-03
0.061
0.000此处所载数值的范围0.745
职业群单位数值
尺度 · 母数 · 来源
观测暴露度指数，按发布原值0–1
以O*NET任务映射为基准
按 SOC 2018 职业发布的数值；具有相同 SOC 2018 代码的所有 O*NET 职业均显示此值
来源数据集（CSV 文件下载）
数据来源: ILO发布时间: 2025
0.40
0.09此处所载数值的范围0.70
职业群单位数值
尺度 · 母数 · 来源
生成式AI暴露度指数，按发布原值0–1
按 ISCO-08 细类（4 位）发布的数值。按原样应用美国劳工统计局（BLS）的官方对照表（ISCO-08→2010 SOC、2010 SOC→2018 SOC）关联到本职业，对应关系为全部或部分对应
来源数据集（PDF 文件下载）

该来源发布的是什么性质的数值

BLS的类别是相对排位而非绝对水平，也不是一手测量：它把多项已发表研究给出的职业百分位排名归并为四个等级。它不是就业或工资预测，不是采用概率，也不区分自动化与增强。

Task-level exposure

仅显示有暴露的工作

已评分任务 33 项 · β ≥ 0.5 的任务 30 项（90.9%）

β = 直接暴露（E1）+ 0.5 × 借助工具时的暴露（E2），依据原始代码库的定义。

原始单位：O*NET 27.2 任务 → O*NET 31.0 职业代码
所有已评分任务均在 O*NET 31.0 任务列表中。

来源: OpenAI "GPTs are GPTs" exposure rubric
版本: gh-main-0471612
许可: MIT License, Copyright (c) 2024 OpenAI

Task (O*NET 20.1)	Claude.aiRaw / share %
Code, evaluate, or interpret collected study data. 11-9121.01	0.030032.4
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, and potential subject risks. 11-9121.01	0.014115.2
Prepare study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. 11-9121.01	0.012013.0
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics. 11-9121.01	0.00788.5
Inform patients or caregivers about study aspects and outcomes to be expected. 11-9121.01	0.00667.2
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. 11-9121.01	0.00657.0
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. 11-9121.01	0.00576.2
Participate in the development of study protocols including guidelines for administration or data collection procedures. 11-9121.01	0.00404.4
Communicate with laboratories or investigators regarding laboratory findings. 11-9121.01	0.00343.7
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions. 11-9121.01	0.00232.5
Not observed on any surface — 23 task(s) — These tasks have no row in the source for this release. The 0 in the share row is a display-stage composition ratio; absence is what the — in the raw row states.
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.	—0
Participate in preparation and management of research budgets and monetary disbursements.	—0
Confer with health care professionals to determine the best recruitment practices for studies.	—0
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.	—0
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.	—0
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.	—0
Order drugs or devices necessary for study completion.	—0
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.	—0
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, and discussions with physicians and nurses.	—0
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.	—0
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.	—0
Solicit industry-sponsored trials through contacts and professional organizations.	—0
Register protocol patients with appropriate statistical centers as required.	—0
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.	—0
Develop advertising and other informational materials to be used in subject recruitment.	—0
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.	—0
Organize space for study equipment and supplies.	—0
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.	—0
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.	—0
Direct the requisition, collection, labeling, storage, or shipment of specimens.	—0
Contact outside health care providers and communicate with subjects to obtain follow-up information.	—0
Arrange for research study sites and determine staff or equipment availability.	—0
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.	—0

Values in this tab are predicted labels, not observations. Eloundou et al. (2023) published two rating regimes — human raters and GPT-4 — and the β shown here is derived from the GPT-4 rater basis alone; the same task can take a different value under the other regime. The unit and the meaning differ from the observed shares (%) in the other tabs, so do not place them on the same axis.

Task (O*NET 27.2)	βE1 + 0.5 × E2
Register protocol patients with appropriate statistical centers as required. O*NET Task ID 15584	1.0
Develop advertising and other informational materials to be used in subject recruitment. O*NET Task ID 15589	1.0
Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. O*NET Task ID 15595	1.0
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data. O*NET Task ID 15600	1.0
Code, evaluate, or interpret collected study data. O*NET Task ID 15609	1.0
Solicit industry-sponsored trials through contacts and professional organizations. O*NET Task ID 15582	0.5
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues. O*NET Task ID 15583	0.5
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. O*NET Task ID 15585	0.5
Participate in preparation and management of research budgets and monetary disbursements. O*NET Task ID 15586	0.5
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics. O*NET Task ID 15588	0.5
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion. O*NET Task ID 15590	0.5
Confer with health care professionals to determine the best recruitment practices for studies. O*NET Task ID 15591	0.5
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts. O*NET Task ID 15592	0.5
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks. O*NET Task ID 15593	0.5
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies. O*NET Task ID 15594	0.5
Participate in the development of study protocols including guidelines for administration or data collection procedures. O*NET Task ID 15596	0.5
Oversee subject enrollment to ensure that informed consent is properly obtained and documented. O*NET Task ID 15597	0.5
Order drugs or devices necessary for study completion. O*NET Task ID 15598	0.5
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures. O*NET Task ID 15601	0.5
Inform patients or caregivers about study aspects and outcomes to be expected. O*NET Task ID 15602	0.5
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions. O*NET Task ID 15603	0.5
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary. O*NET Task ID 15604	0.5
Contact outside health care providers and communicate with subjects to obtain follow-up information. O*NET Task ID 15606	0.5
Communicate with laboratories or investigators regarding laboratory findings. O*NET Task ID 15607	0.5
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. O*NET Task ID 15608	0.5
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses. O*NET Task ID 15610	0.5
Arrange for research study sites and determine staff or equipment availability. O*NET Task ID 15611	0.5
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols. O*NET Task ID 15612	0.5
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices. O*NET Task ID 15613	0.5
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms. O*NET Task ID 15614	0.5
再显示 20 项工作 ▾收起 ▴
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms. O*NET Task ID 15587	0.0
Organize space for study equipment and supplies. O*NET Task ID 15599	0.0
Direct the requisition, collection, labeling, storage, or shipment of specimens. O*NET Task ID 15605	0.0

β = E1 + 0.5 × E2 · E1 = tasks where direct LLM access alone cuts time by at least 50%, E2 = tasks where software built on top of an LLM cuts time by at least 50%. Values take only 0 / 0.5 / 1.0.

Data sources & licenses — O*NET®, Anthropic Economic Index, Eloundou et al. (2023): see full notices on the Credits page

O*NET 31.0 全部任务（33 项）

本职业在 O*NET 31.0 中的全部任务（英文原文；任务类型为核心或补充）。暴露值不列在此清单中，而在上方表格里，位于各来源所用 O*NET 版本的任务表述旁。

任务（O*NET 31.0）	类型
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.	核心
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.	核心
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.	核心
Develop advertising and other informational materials to be used in subject recruitment.	核心
Confer with health care professionals to determine the best recruitment practices for studies.	核心
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.	核心
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.	核心
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.	核心
Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.	核心
Participate in the development of study protocols including guidelines for administration or data collection procedures.	核心
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.	核心
Order drugs or devices necessary for study completion.	核心
Organize space for study equipment and supplies.	核心
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.	核心
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.	核心
Inform patients or caregivers about study aspects and outcomes to be expected.	核心
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.	核心
Direct the requisition, collection, labeling, storage, or shipment of specimens.	核心
Contact outside health care providers and communicate with subjects to obtain follow-up information.	核心
Communicate with laboratories or investigators regarding laboratory findings.	核心
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.	核心
Code, evaluate, or interpret collected study data.	核心
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.	核心
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.	核心
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.	核心
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.	核心
Solicit industry-sponsored trials through contacts and professional organizations.	补充
Register protocol patients with appropriate statistical centers as required.	补充
Participate in preparation and management of research budgets and monetary disbursements.	补充
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.	补充
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.	补充
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.	补充
Arrange for research study sites and determine staff or equipment availability.	补充

Anthropic「What work can robots do?」2026-09

0.06/ 3· 机器人暴露指数

0 不可3 非结构化环境

尺度 · 母数 · 来源

对每项体力任务，按已实际部署、销售或演示的机器人能够完成它的环境评定 0–3 级（0 不可 · 1 围栏式机器单元、灌装线等机器人专用设施 · 2 医院药房、集装箱港口等受管理的设施 · 3 私人住宅、建筑工地等非结构化环境），再按工作时间占比求平均

以该职业 O*NET 29.3 任务中的体力任务为准

等级与时间占比由 Anthropic 使用 Claude Opus 5（网络搜索）估算（截至 2026 年）。

来源数据集

机器人暴露指数与本站的 AI 暴露度是不同的指标，不能相加或相互比较。该指数不代表实际采用情况或成本竞争力，0 也包括没有体力任务的职业。

每项体力任务的等级

机器人环境等级（E0–E3）

E0 机器人不可详情
评定为已实际部署、销售或演示的机器人即使在机器人专用设施中也无法完成
E1 机器人专用设施详情
评定为可在围绕机器搭建的设施中完成，例如围栏式机器单元或灌装线
E2 受管理的设施详情
评定为可在由机构按工作标准维护的人类工作设施中完成，例如医院药房或集装箱港口
E3 非结构化环境详情
评定为可在没有机构按工作标准维护的环境中完成，例如私人住宅或建筑工地

仅列出被归类为体力任务的任务；其他任务在来源中没有等级。

任务（O*NET 29.3）	机器人环境等级
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.	E0 机器人不可
Organize space for study equipment and supplies.	E1 机器人专用设施
Direct the requisition, collection, labeling, storage, or shipment of specimens.	E1 机器人专用设施
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.	E1 机器人专用设施

就业展望（BLS）

这些数值属于整个 SOC 11-9121 组（Natural sciences managers），并非仅属于该 O*NET 职业。

就业人数，2025: 112K
预计就业人数，2035: 122K
变化 (2025–35): +8.2%
年薪中位数，2025: $167,220
入职通常所需学历: Bachelor's degree

最低 $30,890BLS EP 2025–35 中 825 个细分职业的工资中位数范围最高 $559,030

来源: U.S. Bureau of Labor Statistics, Employment Projections 2025–35 — Employment by detailed occupation, 2025 and projected 2035

韩国职业分类关联（KSCO）

来自 AI Changing Work 制作的 Korea Occupation Direct Crosswalk v1.1 当前版本的关联。关系值从 O*NET-SOC 职业一侧解读。

KSCO 代码	KSCO 名称	关系	状态
13113	생명 및 자연과학 연구 관리자	相关，但不对应	已确认

关系与状态的定义(kr-direct v1.1)

国际劳工组织（ILO）职业说明

以下 ISCO-08 职业组由 AI Changing Work 原样套用美国劳工统计局（BLS）发布的对照表（2018 SOC→2010 SOC、2010 SOC→ISCO-08）、不逐案取舍，与本职业相关联；每项关联可能是完全对应，也可能是部分对应。

ISCO-08 1223Research and Development Managers
研究与开发经理

自行翻译

自行翻译 · 非 ISCO 官方词汇 — 未经国际劳工组织审核。

以下定义、任务和职业示例是 ILO 对该 ISCO-08 职业组的描述，而不是对本职业的描述。

Research and development managers plan, direct and coordinate the research and development activities of an enterprise or organization or of enterprises that provide related services to other enterprises and organizations.

任务

(a) planning, directing and coordinating research and development activities, in-house or commissioned from external research organizations, to develop new or improved technical processes, products, knowledge, or utilization of materials;
(b) planning the overall research and development programme of an enterprise or organization, specifying goals and budgetary requirements;
(c) leading and managing the activities of research and development staff;
(d) establishing and managing budgets, controlling expenditure and ensuring the efficient use of resources;
(e) establishing and directing operational and administrative procedures;
(f) planning and directing daily operations;
(g) overseeing the selection, training and performance of staff;
(h) representing the enterprise or organization at conventions, seminars and conferences.

职业示例

Product development manager · Research manager

Sources: ILO ISCO-08 — details: Credits

ESCO 职业词汇

以下每一项都是在已公开的ESCO-O*NET Crosswalk（第 1 版，2022 年）中与本职业逐项对应的。对应类型出自该对照表；表述出自 AI Changing Work。

research managerESCO 1223.2.2本职业范围更窄
Research managers oversee the research and development functions of a research facility or program or university. They support the executive staff, coordinate work activities, and monitor staff and research projects. They may work in a wide array of sectors, such as the chemical, technical and life sciences sector. Research managers can also advise on research and execute research themselves.

来源: European Commission, DG EMPL — ESCO API 2026-08-08 (bridge v1.2.1)

许可: CC BY 4.0 (EU Reuse Notice)

查看原文

ESCO reuse terms and the modification notice are in Credits.

法国职业分类关联（ROME）

本职业与 ROME 4.0 职业条目（fiche）之间的关联，由 AI Changing Work 借助 AI 模型判定。关系从本职业一侧解读。标为「暂定」的关联仅凭同一模型系列（Claude）两位判定者的判定采纳，或对其判定适用运营方规则后采纳，因此其依据弱于已确认的关联。

ROME 代码	ROME 名称（法语）	关系
H1211	Attaché / Attachée de recherche clinique (ARC)	本职业范围更宽
H1213	Responsable du développement clinique en industrie pharmaceutique	本职业范围更宽
H1219	Responsable opérationnel / Responsable opérationnelle des études cliniques en industrie pharmaceutique	本职业范围更宽
H1223	Coordinateur / Coordinatrice d'études cliniques en industrie pharmaceutique	本职业范围更宽
K2405	Attaché / Attachée de recherche clinique en milieu hospitalier	有重叠，但不相同
H1222	Responsable médical / Responsable médicale des études cliniques en industrie pharmaceutique	相关，但不对应暂定

Source: France Travail — Répertoire Opérationnel des Métiers et des Emplois (ROME 4.0), version 61, last updated 15 June 2026 (https://www.data.gouv.fr/datasets/repertoire-operationnel-des-metiers-et-des-emplois-rome). Licence Ouverte 2.0.

ROME codes and titles are reproduced unchanged; the links to O*NET-SOC occupations are AI Changing Work's own judgment and are not a France Travail correspondence.

(AI Changing Work link release: fr-direct v1)

西班牙职业分类关联（CNO-11）

本职业与 CNO-11 职业之间的关联，由 AI Changing Work 借助 AI 模型判定。关系从本职业一侧解读。

CNO-11 代码	CNO-11 名称（西班牙语）	关系
1223	Directores de investigación y desarrollo	相关，但不对应

Source: Instituto Nacional de Estadística (INE), National Classification of Occupations 2011 (CNO-11, Royal Decree 1591/2010) — www.ine.es · Licensed CC BY 4.0. CNO-11 codes and Spanish titles are reproduced unchanged; the links to O*NET occupations are AI Changing Work's own judgment and are not an INE correspondence.

(AI Changing Work link release: es-direct v1)

德国职业分类关联（KldB）

本职业与 KldB 职业之间的关联，由 AI Changing Work 借助 AI 模型判定。关系从本职业一侧解读。

KldB 代码	KldB 名称（德语）	关系
81884	Berufe in der Pharmazie (sonstige spezifische Tätigkeitsangabe) - hoch komplexe Tätigkeiten	有重叠，但不相同暂定
73342	Berufe in der medizinischen Dokumentation - fachlich ausgerichtete Tätigkeiten	相关，但不对应暂定

Source: © Statistik der Bundesagentur für Arbeit — Klassifikation der Berufe 2010 – überarbeitete Fassung 2020, https://statistik.arbeitsagentur.de. KldB codes and titles are reproduced unchanged; the links to O*NET occupations are AI Changing Work's own mapping (eigene Zuordnung) and are not a Bundesagentur für Arbeit correspondence.

(AI Changing Work link release: de-direct v1)

日本职业分类关联（JSCO）

本职业与 JSCO 职业之间的关联，由 AI Changing Work 借助 AI 模型判定。关系从本职业一侧解读。

JSCO 代码	JSCO 名称（日语）	关系
159	他に分類されない保健医療従事者	本职业范围更窄

Source: Ministry of Internal Affairs and Communications (MIC), Japan Standard Occupational Classification (Dec. 2009, MIC Notification No. 555). JSCO codes and Japanese titles are reproduced unchanged; the links to O*NET occupations are AI Changing Work's own judgment and are not a MIC correspondence.

(AI Changing Work link release: jp-direct v1)

本页数据的来源与许可，以及 AI Changing Work 的修改与翻译说明：致谢与来源