Regulatory Affairs Managers

O*NET-SOC 代码: 11-9199.01

Plan, direct, or coordinate production activities of an organization to ensure compliance with regulations and standard operating procedures.

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
0.069
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
0.32–0.42· ISCO-08 职业组 6 个
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。

各关联 ISCO-08 职业组的 ILO 数值

ISCO-08 1114Senior Officials of Special-interest Organizations0.37
ISCO-08 1213Policy and Planning Managers0.36
ISCO-08 1219Business Services and Administration Managers Not Elsewhere Classified0.42
ISCO-08 1322Mining Managers0.35
ISCO-08 1349Professional Services Managers Not Elsewhere Classified0.38
ISCO-08 1431Sports, Recreation and Cultural Centre Managers0.32

Task-level exposure

仅显示有暴露的工作

已评分任务 27 项 · β ≥ 0.5 的任务 27 项（100.0%）

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 %	APIRaw / share %
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products. 11-9199.01	0.008129.0	0.005511.3
Review materials such as marketing literature or user manuals to ensure that regulatory agency requirements are met. 11-9199.01	0.007727.6	0.023649.0
Represent organizations before domestic or international regulatory agencies on major policy matters or decisions regarding company products. 11-9199.01	0.004114.7	0.00428.8
Review all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards. 11-9199.01	0.00248.6	0.007315.2
Investigate product complaints and prepare documentation and submissions to appropriate regulatory agencies as necessary. 11-9199.01	0.00207.2	0.00479.9
Establish procedures or systems for publishing document submissions either in hardcopy or electronic formats. 11-9199.01	0.00207.2	—0
Maintain current knowledge of relevant regulations, including proposed and final rules. 11-9199.01	0.00165.7	0.00285.8
Not observed on any surface — 20 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.
Direct the preparation and submission of regulatory agency applications, reports, or correspondence.	—0	—0
Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced.	—0	—0
Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.	—0	—0
Develop regulatory strategies and implementation plans for the preparation and submission of new products.	—0	—0
Establish regulatory priorities or budgets and allocate resources and workloads.	—0	—0
Implement or monitor complaint processing systems to ensure effective and timely resolution of all complaint investigations.	—0	—0
Manage activities such as audits, regulatory agency inspections, or product recalls.	—0	—0
Monitor emerging trends regarding industry regulations to determine potential impacts on organizational processes.	—0	—0
Oversee documentation efforts to ensure compliance with domestic and international regulations and standards.	—0	—0
Participate in the development or implementation of clinical trial protocols.	—0	—0
Provide responses to regulatory agencies regarding product information or issues.	—0	—0
Train staff in regulatory policies or procedures.	—0	—0
Contribute to the development or implementation of business unit strategic and operating plans.	—0	—0
Develop and maintain standard operating procedures or local working practices.	—0	—0
Coordinate internal discoveries and depositions with legal department staff.	—0	—0
Evaluate new software publishing systems and confer with regulatory agencies concerning news or updates related to electronic publishing of submissions.	—0	—0
Develop relationships with state or federal environmental regulatory agencies to learn about and analyze the potential impacts of proposed environmental policy regulations.	—0	—0
Evaluate regulatory affairs aspects that are specifically green, such as the use of toxic substances in packaging, carbon footprinting issues, or green policy implementation.	—0	—0
Monitor regulatory affairs activities to ensure that they are aligned with corporate sustainability or green initiatives.	—0	—0
Monitor regulatory affairs trends that are related to environmental issues.	—0	—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
Review materials such as marketing literature or user manuals to ensure that regulatory agency requirements are met. O*NET Task ID 18038	1.0
Develop and maintain standard operating procedures or local working practices. O*NET Task ID 18042	1.0
Establish procedures or systems for publishing document submissions in hardcopy or electronic formats. O*NET Task ID 18043	1.0
Direct the preparation and submission of regulatory agency applications, reports, or correspondence. O*NET Task ID 18022	0.5
Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced. O*NET Task ID 18023	0.5
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products. O*NET Task ID 18024	0.5
Communicate regulatory information to multiple departments and ensure that information is interpreted correctly. O*NET Task ID 18025	0.5
Develop regulatory strategies and implementation plans for the preparation and submission of new products. O*NET Task ID 18026	0.5
Establish regulatory priorities or budgets and allocate resources and workloads. O*NET Task ID 18027	0.5
Implement or monitor complaint processing systems to ensure effective and timely resolution of all complaint investigations. O*NET Task ID 18028	0.5
Investigate product complaints and prepare documentation and submissions to appropriate regulatory agencies as necessary. O*NET Task ID 18029	0.5
Maintain current knowledge of relevant regulations, including proposed and final rules. O*NET Task ID 18030	0.5
Manage activities such as audits, regulatory agency inspections, or product recalls. O*NET Task ID 18031	0.5
Monitor emerging trends regarding industry regulations to determine potential impacts on organizational processes. O*NET Task ID 18032	0.5
Participate in the development or implementation of clinical trial protocols. O*NET Task ID 18034	0.5
Provide responses to regulatory agencies regarding product information or issues. O*NET Task ID 18035	0.5
Represent organizations before domestic or international regulatory agencies on major policy matters or decisions regarding company products. O*NET Task ID 18036	0.5
Review all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards. O*NET Task ID 18037	0.5
Train staff in regulatory policies or procedures. O*NET Task ID 18039	0.5
Contribute to the development or implementation of business unit strategic and operating plans. O*NET Task ID 18040	0.5
Coordinate internal discoveries and depositions with legal department staff. O*NET Task ID 18041	0.5
Evaluate new software publishing systems and confer with regulatory agencies concerning news or updates on electronic publishing of submissions. O*NET Task ID 18044	0.5
Develop relationships with state or federal environmental regulatory agencies to learn about and analyze the potential impacts of proposed environmental policy regulations. O*NET Task ID 19529	0.5
Evaluate regulatory affairs aspects that are specifically green, such as the use of toxic substances in packaging, carbon footprinting issues, or green policy implementation. O*NET Task ID 19530	0.5
Monitor regulatory affairs activities to ensure their alignment with corporate sustainability or green initiatives. O*NET Task ID 19531	0.5
Monitor regulatory affairs trends related to environmental issues. O*NET Task ID 19532	0.5
Direct documentation efforts to ensure compliance with domestic and international regulations and standards. O*NET Task ID 21087	0.5
再显示 17 项工作 ▾收起 ▴

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（27 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
Direct the preparation and submission of regulatory agency applications, reports, or correspondence.	核心
Formulate or implement regulatory affairs policies and procedures to ensure that regulatory compliance is maintained or enhanced.	核心
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.	核心
Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.	核心
Develop regulatory strategies and implementation plans for the preparation and submission of new products.	核心
Establish regulatory priorities or budgets and allocate resources and workloads.	核心
Implement or monitor complaint processing systems to ensure effective and timely resolution of all complaint investigations.	核心
Investigate product complaints and prepare documentation and submissions to appropriate regulatory agencies as necessary.	核心
Maintain current knowledge of relevant regulations, including proposed and final rules.	核心
Manage activities such as audits, regulatory agency inspections, or product recalls.	核心
Monitor emerging trends regarding industry regulations to determine potential impacts on organizational processes.	核心
Participate in the development or implementation of clinical trial protocols.	核心
Provide responses to regulatory agencies regarding product information or issues.	核心
Represent organizations before domestic or international regulatory agencies on major policy matters or decisions regarding company products.	核心
Review all regulatory agency submission materials to ensure timeliness, accuracy, comprehensiveness, or compliance with regulatory standards.	核心
Review materials such as marketing literature or user manuals to ensure that regulatory agency requirements are met.	核心
Train staff in regulatory policies or procedures.	核心
Contribute to the development or implementation of business unit strategic and operating plans.	核心
Coordinate internal discoveries and depositions with legal department staff.	核心
Develop and maintain standard operating procedures or local working practices.	核心
Establish procedures or systems for publishing document submissions in hardcopy or electronic formats.	核心
Develop relationships with state or federal environmental regulatory agencies to learn about and analyze the potential impacts of proposed environmental policy regulations.	核心
Evaluate regulatory affairs aspects that are specifically green, such as the use of toxic substances in packaging, carbon footprinting issues, or green policy implementation.	核心
Monitor regulatory affairs activities to ensure their alignment with corporate sustainability or green initiatives.	核心
Monitor regulatory affairs trends related to environmental issues.	核心
Direct documentation efforts to ensure compliance with domestic and international regulations and standards.	核心
Evaluate new software publishing systems and confer with regulatory agencies concerning news or updates on electronic publishing of submissions.	补充

就业展望（BLS）

这些数值属于整个 SOC 11-9199 组（Managers, all other），并非仅属于该 O*NET 职业。

就业人数，2025: 1.3M
预计就业人数，2035: 1.4M
变化 (2025–35): +4.9%
年薪中位数，2025: $141,900
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
12129	그 외 경영 지원 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 1114Senior Officials of Special-interest Organizations
特殊利益团体高级官员
ISCO-08 1213Policy and Planning Managers
政策和规划经理
ISCO-08 1219Business Services and Administration Managers Not Elsewhere Classified
其他未列明的商务服务和行政管理人员
ISCO-08 1322Mining Managers
采矿业经理
ISCO-08 1349Professional Services Managers Not Elsewhere Classified
其他未列明的专业服务经理
ISCO-08 1431Sports, Recreation and Cultural Centre Managers
体育、娱乐和文化中心经理
ISCO-08 1439Services Managers Not Elsewhere Classified
其他未列明的服务业经理

自行翻译

自行翻译 · 非 ISCO 官方词汇 — 未经国际劳工组织审核。

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。

regulatory affairs managerESCO 2619.10范围相同
Regulatory affairs managers are in charge of regulatory and legal affairs in several sectors such as the healthcare, energy and banking industries. They oversee the development of products and services from inception to market release by making sure everything complies with the local legislation and meets regulatory requirements. They have experience in the different phases of regulatory processes and act as an interface between business and government legislation or regulatory boards.

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
H1509	Responsable des affaires règlementaires en industrie pharmaceutique	本职业范围更宽
H1507	Chargé / Chargée des affaires réglementaires	有重叠，但不相同
H1104	Directeur / Directrice des affaires médicales pharmaceutiques	相关，但不对应
H1513	Responsable de pharmacovigilance en industrie pharmaceutique	相关，但不对应

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
1219	Directores de políticas y planificación y de otros departamentos administrativos no clasificados bajo otros epígrafes	本职业范围更窄

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
81894	Führungskräfte - Pharmazie	相关，但不对应

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
031	会社管理職員	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