Regulatory Affairs Specialists
Business and Financial Operations Occupations- O*NET-SOC コード
- 13-1041.07
Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals, or registrations. May compile and prepare materials for submission to regulatory agencies.
職業名とタスク記述は、公表された英語のまま表示します。ラベル（タスクの種類を含む）は翻訳しています。
AI露出度
- データ出典: BLS公表時点: 2026-08
非常に高い· 相対
低い4段階の相対区分非常に高い職業群単位の値
尺度・母数・出典
4段階の相対区分（低い / 中程度 / 高い / 非常に高い）
BLS雇用見通し表の詳細職業831件が母数。値は NEM(全国雇用マトリクス)コード単位で付与されるため、同じ NEM コードの職業は同じバンドになります
- データ出典: Anthropic公表時点: 2026-03
0.121
0.000ここに掲載された値の範囲0.745職業群単位の値
尺度・母数・出典
観測エクスポージャー指数、公開されたまま0–1
O*NETタスクへの対応づけが基準
SOC 2018の職業単位で公表された値で、同じSOC 2018コードを持つO*NET職業はすべてこの値になります
- データ出典: ILO公表時点: 2025
0.32–0.45· ISCO-08職業グループ3件
尺度・母数・出典
生成AI露出度指数、公開されたまま0–1
ISCO-08の細分類（4桁）単位で公表された値です。米国労働統計局（BLS）の公式対応表（ISCO-08→2010 SOC、2010 SOC→2018 SOC）を公表どおり適用してこの職業に結び付けており、対応は全部または一部です
この出典がどのような性格の値か
BLSの区分は絶対水準ではなく相対順位であり、一次測定でもありません。複数の既存研究が付けた職業別パーセンタイル順位を4段階にまとめた値です。雇用や賃金の予測でもなく、導入確率でもなく、自動化と増強を区別しません。
結び付けたISCO-08グループごとのILO値
- ISCO-08 3351Customs and Border Inspectors0.32
- ISCO-08 3353Government Social Benefits Officials0.45
- ISCO-08 3354Government Licensing Officials0.43
AI 曝露度（OpenAI ルーブリック）
評価済みタスク 32 件 · β ≥ 0.5 のタスク 31 件（96.9%）
β = 直接的な露出（E1）+ 0.5 × ツール利用時の露出（E2）。原典リポジトリの定義に従います。
- 原典の単位：O*NET 27.2 のタスク → O*NET 31.0 の職業コード
- 評価済みタスクのうち 3 件は O*NET 31.0 のタスク一覧になく、O*NET 27.2 基準で公表されたスコアをそのまま残しています。
- 出典
- OpenAI "GPTs are GPTs" exposure rubric
- 版
- gh-main-0471612
- ライセンス
- MIT License, Copyright (c) 2024 OpenAI
タスク
O*NET® 31.0 Database のタスク記述です。コアタスクを先に表示します。
| タスク | 種類 | β（OpenAI） |
|---|---|---|
| Communicate with regulatory agencies regarding pre-submission strategies, potential regulatory pathways, compliance test requirements, or clarification and follow-up of submissions under review. | コア | 0.5 |
| Coordinate, prepare, or review regulatory submissions for domestic or international projects. | コア | 0.5 |
| Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures. | コア | 0.5 |
| Provide technical review of data or reports to be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation. | コア | 1 |
| Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies. | コア | 0.5 |
| Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues. | コア | 0.5 |
| Compile and maintain regulatory documentation databases or systems. | コア | 0.5 |
| Coordinate efforts associated with the preparation of regulatory documents or submissions. | コア | 0.5 |
| Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed device changes or labeling changes. | コア | 0.5 |
| Develop or conduct employee regulatory training. | コア | 0.5 |
| Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents. | コア | 0.5 |
| Obtain and distribute updated information regarding domestic or international laws, guidelines, or standards. | コア | 0.5 |
| Participate in internal or external audits. | コア | 0.5 |
| Prepare or direct the preparation of additional information or responses as requested by regulatory agencies. | コア | 0.5 |
| Prepare or maintain technical files as necessary to obtain and sustain product approval. | コア | 0.5 |
| Recommend changes to company procedures in response to changes in regulations or standards. | コア | 0.5 |
| Prepare responses to customer requests for information, such as product data, written regulatory affairs statements, surveys, or questionnaires. | コア | 1 |
| Review clinical protocols to ensure collection of data needed for regulatory submissions. | コア | 0.5 |
| Write or update standard operating procedures, work instructions, or policies. | コア | 1 |
| Coordinate recall or market withdrawal activities as necessary. | コア | 0.5 |
| Develop or track quality metrics. | コア | 0.5 |
| Review adverse drug reactions and file all related reports in accordance with regulatory agency guidelines. | コア | 0.5 |
| Identify relevant guidance documents, international standards, or consensus standards. | コア | 0.5 |
| Provide pre-, ongoing, and post-inspection follow-up assistance to governmental inspectors. | コア | 0.5 |
| Develop regulatory strategies for products. | コア | 未評価 |
| Direct the collection and preparation of laboratory samples as requested by regulatory agencies. | 補足 | 0 |
| Determine regulations or procedures related to the management, collection, reuse, recovery, or recycling of packaging waste. | 補足 | 0.5 |
| Determine requirements applying to treatment, storage, shipment, or disposal of potentially hazardous production-related waste. | 補足 | 0.5 |
| Determine the legal implications of the production, supply, or use of ozone-depleting substances or equipment containing such substances. | 補足 | 0.5 |
| Recommend adjudication of product complaints. | 補足 | 0.5 |
職業情報
出典と帰属表示
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: 13-1041.07 Regulatory Affairs Specialists
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.