Gerentes de Ensaios Clinicos

Gestão

Estamos verificando as ligações de dados desta ocupação; alguns números estão temporariamente ocultos.

Exposição à IA

  • Fonte dos dados: BLSPublicado: 2026-08

    Alto· relativa

    BaixoQuatro faixas relativasMuito alto

    Valor por grupo ocupacional

    Escala, base e fonte

    Quatro faixas relativas (Baixo / Moderado / Alto / Muito alto)

    831 ocupações detalhadas da tabela de projeções de emprego do BLS. O valor é atribuído por código da National Employment Matrix (NEM), pelo que as ocupações que partilham um código NEM recebem a mesma banda

    Conjunto de dados de origem (transferência XLSX)

  • Fonte dos dados: AnthropicPublicado: 2026-03

    0.061

    0.000Intervalo dos valores aqui apresentados0.745
    Escala, base e fonte

    Índice de exposição observada, 0–1 tal como publicado

    Mapeado sobre tarefas O*NET

    Conjunto de dados de origem

  • Fonte dos dados: ILOPublicado: 2025

    0.40

    0.09Intervalo dos valores aqui apresentados0.70

    Valor por grupo ocupacional

    Escala, base e fonte

    Índice de exposição à IA generativa, 0–1 tal como publicado

    Grupo de base CITP-08 — todas as ocupações com o mesmo código recebem este valor

    Calculado por este site, não publicado pela OIT: das 1.012 ocupações que este site liga ao conjunto de dados da OIT, 39% atingem ou superam este valor.

    Conjunto de dados de origem

Que tipo de valor esta fonte publica

A categoria de BLS é uma posição relativa, não um nível absoluto, e também não é uma medição de primeira mão: agrupa em quatro faixas as posições percentis da ocupação em vários estudos publicados. Não é uma previsão de emprego ou de salários, não é uma probabilidade de adoção e não distingue automação de aumento.

Task-level exposure

Apenas tarefas expostas
TaskClaude.aiRaw / share %APIRaw / share %
Code, evaluate, or interpret collected study data.

11-9121

0.030030.00.470071.2
Review project activities and prepare and review research, testing, or operational reports.

11-9121

0.020020.00.190028.8
Advise or assist in obtaining patents or meeting other legal requirements.

11-9121

0.020020.00.00000.0
Develop advertising and other informational materials to be used in subject recruitment.

11-9121

0.010010.00.00000.0
Dispense medical devices or drugs, and calculate dosages and provide instructions as necessary.

11-9121

0.010010.00.00000.0
Design or coordinate successive phases of problem analysis, solution proposals, or testing.

11-9121

0.010010.0—0
Develop client relationships and communicate with clients to explain proposals, present research findings, establish specifications, or discuss project status.

11-9121

0.00000.00.00000.0
Prepare project proposals.

11-9121

0.00000.0—0
Interpret protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.

11-9121

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

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

11-9121

0.00000.0—0
Not observed on any surface — 38 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.
Confer with scientists, engineers, regulators, or others to plan or review projects or to provide technical assistance.
—0—0
Plan or direct research, development, or production activities.
—0—0
Hire, supervise, or evaluate engineers, technicians, researchers, or other staff.
—0—0
Determine scientific or technical goals within broad outlines provided by top management and make detailed plans to accomplish these goals.
—0—0
Develop or implement policies, standards, or procedures for the architectural, scientific, or technical work performed to ensure regulatory compliance or operations enhancement.
—0—0
Develop innovative technology or train staff for its implementation.
—0—0
Conduct own research in field of expertise.
—0—0
Recruit personnel or oversee the development or maintenance of staff competence.
—0—0
Prepare and administer budgets, approve and review expenditures, and prepare financial reports.
—0—0
Make presentations at professional meetings to further knowledge in the field.
—0—0
Provide for stewardship of plant or animal resources or habitats, studying land use, monitoring animal populations, or providing shelter, resources, or medical treatment for animals.
—0—0
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: see full notices on the Credits page

Informação ocupacional