Clinical Research Coordinators

Management Occupations
O*NET-SOC コード
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.

  • データ出典: BLS公表時点: 2026-08

    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

    出典データセット（XLSX ファイルのダウンロード）

  • データ出典: Anthropic公表時点: 2026-03

    0.061

    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

    出典データセット（CSV ファイルのダウンロード）

  • データ出典: ILO公表時点: 2025

    0.40

    0.09ここに掲載された値の範囲0.70

    職業群単位の値

    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

    出典データセット（PDF ファイルのダウンロード）

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。

Task-level exposure

露出のある作業のみ

評価済みタスク 33 件 · β ≥ 0.5 のタスク 30 件（90.9%）

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
  • 評価済みタスクはすべて O*NET 31.0 のタスク一覧にあります。
出典
OpenAI "GPTs are GPTs" exposure rubric
版
gh-main-0471612
ライセンス
MIT License, Copyright (c) 2024 OpenAI
Task (O*NET 30.2)Claude.aiRaw / share %APIRaw / share %
Code, evaluate, or interpret collected study data.

11-9121.01

0.030060.00.4700100.0
Develop advertising and other informational materials to be used in subject recruitment.

11-9121.01

0.010020.00.00000.0
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.

11-9121.01

0.010020.00.00000.0
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.

11-9121.01

0.00000.0—0
Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.

11-9121.01

0.00000.0—0
Identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions.

11-9121.01

0.00000.0—0
Not observed on any surface — 27 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.
Review scientific literature, participate in continuing education activities, or attend conferences and seminars to maintain current knowledge of clinical studies affairs and issues.
—0—0
Prepare for or participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
—0—0
Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
—0—0
Confer with health care professionals to determine the best recruitment practices for studies.
—0—0
Track enrollment status of subjects and document dropout information such as dropout causes and subject contact efforts.
—0—0
Review proposed study protocols to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
—0—0
Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
—0—0
Participate in the development of study protocols including guidelines for administration or data collection procedures.
—0—0
Oversee subject enrollment to ensure that informed consent is properly obtained and documented.
—0—0
Order drugs or devices necessary for study completion.
—0—0
Organize space for study equipment and supplies.
—0—0
Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data.
—0—0
Instruct research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
—0—0
Inform patients or caregivers about study aspects and outcomes to be expected.
—0—0
Direct the requisition, collection, labeling, storage, or shipment of specimens.
—0—0
Contact outside health care providers and communicate with subjects to obtain follow-up information.
—0—0
Communicate with laboratories or investigators regarding laboratory findings.
—0—0
Collaborate with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions.
—0—0
Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
—0—0
Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
—0—0
Monitor study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional polices.
—0—0
Maintain required records of study activity including case report forms, drug dispensation records, or regulatory forms.
—0—0
Solicit industry-sponsored trials through contacts and professional organizations.
—0—0
Register protocol patients with appropriate statistical centers as required.
—0—0
Participate in preparation and management of research budgets and monetary disbursements.
—0—0
Contact industry representatives to ensure equipment and software specifications necessary for successful study completion.
—0—0
Arrange for research study sites and determine staff or equipment availability.
—0—0

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

O*NET 31.0 のタスク全件（33件）

この職業の O*NET 31.0 のタスク全件（英語原文、種別はコア・補足）。露出値はこの一覧には載せず、上の表で各出典が用いた O*NET 版の文言の横にあります。

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

職業情報

雇用見通し（BLS）

この O*NET 職業だけの値ではなく、SOC 11-9121 グループ（Natural sciences managers）全体の値です。

雇用者数、2025
112K
雇用者数見通し、2035
122K
変化率 (2025–35)
+8.2%
年間賃金の中央値、2025
$167,220
入職時に通常必要な学歴
Bachelor's degree
最低 $30,890BLS EP 2025–35 の詳細職業825件の賃金中央値の範囲最高 $559,030

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

韓国職業分類との対応（KSCO）

AI Changing Work が作成した Korea Occupation Direct Crosswalk v1.1 現行版の対応です。関係の値は O*NET-SOC 職業の側から読みます。

KSCO コードKSCO 名称関係状態
13113생명 및 자연과학 연구 관리자関連（対応ではない）確定

関係と状態の定義(kr-direct v1.1)

ILO（国際労働機関）の職業説明

以下のISCO-08職業群は、AI Changing Workが米国労働統計局（BLS）の発行するクロスウォーク（2018 SOC→2010 SOC、2010 SOC→ISCO-08）を個別の選択なしにそのまま適用して、この職業に結び付けたものです。結び付きは全体的な対応の場合も部分的な対応の場合もあります。

  • ISCO-08 1223Research and Development Managers

    研究開発管理者

出典: 総務省「国際標準職業分類（ISCO）2008年改定版（仮訳）分類項目名一覧（和英対照）」— 原著：ILO ISCO-08 © International Labour Organization（日本語訳は総務省がILOの許可を得て作成）

原文を見る

以下の定義・作業・職業例は、この職業ではなく、当該ISCO-08職業群についてのILOによる説明です。

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.

作業

  • (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.

職業例

Product development manager · Research manager

Sources: ILO ISCO-08 — details: Credits

ESCO 職業語彙

以下の各項目は、公開されているESCO-O*NET Crosswalk（バージョン1、2022年）で、この職業と一つずつ対応付けられたものです。対応の種類はそのクロスウォークによるもので、表現はAI Changing Workによるものです。

  • research managerESCO 1223.2.2この職業のほうが狭い

    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.

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

ライセンス: CC BY 4.0 (EU Reuse Notice)

原文を見る

ESCO reuse terms and the modification notice are in Credits.

フランス職業分類との対応（ROME）

この職業と ROME 4.0 の職業票（fiche）との対応で、AI Changing Work が AI モデルを用いて判定したものです。関係はこの職業の側から読みます。「暫定」と表示した対応は、同じモデル系列（Claude）の二人の判定者による判定のみ、またはその判定に運営者の規則を適用して採用したものであり、確定した対応より根拠が弱くなります。

ROME コードROME 名称（フランス語）関係
H1211Attaché / Attachée de recherche clinique (ARC)この職業のほうが広い
H1213Responsable du développement clinique en industrie pharmaceutiqueこの職業のほうが広い
H1219Responsable opérationnel / Responsable opérationnelle des études cliniques en industrie pharmaceutiqueこの職業のほうが広い
H1223Coordinateur / Coordinatrice d'études cliniques en industrie pharmaceutiqueこの職業のほうが広い
K2405Attaché / Attachée de recherche clinique en milieu hospitalier重なるが同じではない
H1222Responsable médical / Responsable médicale des études cliniques en industrie pharmaceutique関連（対応ではない）暫定

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)

スペイン職業分類との対応（CNO-11）

この職業と CNO-11 の職業との対応で、AI Changing Work が AI モデルを用いて判定したものです。関係はこの職業の側から読みます。

CNO-11 コードCNO-11 名称（スペイン語）関係
1223Directores de investigación y desarrollo関連（対応ではない）

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)

ドイツ職業分類との対応（KldB）

この職業と KldB の職業との対応で、AI Changing Work が AI モデルを用いて判定したものです。関係はこの職業の側から読みます。

KldB コードKldB 名称（ドイツ語）関係
81884Berufe in der Pharmazie (sonstige spezifische Tätigkeitsangabe) - hoch komplexe Tätigkeiten重なるが同じではない暫定
73342Berufe in der medizinischen Dokumentation - fachlich ausgerichtete Tätigkeiten関連（対応ではない）暫定

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)

日本職業分類との対応（JSCO）

この職業と JSCO の職業との対応で、AI Changing Work が AI モデルを用いて判定したものです。関係はこの職業の側から読みます。

JSCO コードJSCO 名称（日本語）関係
159他に分類されない保健医療従事者この職業のほうが狭い

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)

このページのデータの出典・ライセンスと AI Changing Work による改変・翻訳の告知：クレジットと出典