Part-Time Clinical Rating Specialist | Trials & Assessments

American Clinical Research Services Opco LLC

Houston (TX)

Presencial

USD 90 000 - 138 000

Tempo parcial

14 dias+

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Resumo da oferta

Empathx is seeking a part-time Clinical Rater in Houston, TX to administer and score rating scales, conduct structured interviews, and manage assessments within sponsor guidelines. The role emphasizes data accuracy, safety reporting, and regulatory compliance in a multi-site clinical trial environment.

Responsibilities include maintaining inter-rater reliability, documenting results in EDC, and coordinating with the clinical team.

Qualificações

  • Master's degree or higher in psychology, counseling, neuropsychology, social work, or a related field.
  • PhD, PsyD, or MD preferred.
  • Experience administering psychometric or rating scales in clinical research or practice.
  • Experience in industry-sponsored interventional clinical trials.
  • On-site work in Houston, TX with occasional travel to Dallas site.

Responsabilidades

  • Administer and score validated rating scales per sponsor protocols and rater training.
  • Conduct structured and semi-structured interviews with study participants.
  • Perform baseline, post-baseline, and follow-up assessments per study protocols.
  • Maintain data integrity and inter-rater reliability through calibration and training.
  • Document results in source documents and EDC systems within required timelines.
  • Ensure adherence to blinding procedures and regulatory requirements.

Conhecimentos

Clinical rating
Structured interviews
Documentation
HIPAA compliance

Formação académica

Master's degree or higher
Doctoral degree preferred

Ferramentas

EDC systems
RealTime CTMS
EMR/EHR

Descrição da oferta de emprego

Empathx is seeking a part-time Clinical Rater in Houston, TX to administer and score rating scales, conduct structured interviews, and manage assessments within sponsor guidelines. The role emphasizes data accuracy, safety reporting, and regulatory compliance in a multi-site clinical trial environment.

Responsibilities include maintaining inter-rater reliability, documenting results in EDC, and coordinating with the clinical team.

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