Clinical Psychometric Rater for Mental Health Trials

Alcanza Clinical Research, LLC

Decatur (GA)

Vor Ort

USD 52.000 - 78.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical insurance
401k with match
Dental & Vision

Zusammenfassung

Alcanza Clinical Research, LLC in Decatur, GA, seeks a Clinical Rater to interview participants for multi-site trials across ADHD, Alzheimer's, MDD and more, ensuring compliance with FDA, GCP and HIPAA.

The role emphasizes prescreening, administering standardized scales, documenting findings, and maintaining ALCOA-C source records, with opportunities for certification and professional growth.

Qualifikationen

  • Master’s degree with 1+ year experience performing psychometric rating scales in a clinical setting or clinical trials.
  • Certifications to rate scales (SCID-5-CT, MINI, LSAS, HAM-A/D, C-SSRS, MADRS, MGH-ATRQ, ISI, CGI, HDRS-17, PANSS, YMRS, ADAS-Cog, CDR, MMSE, RBANS, MOCA) are highly preferred.

Aufgaben

  • Review medical history and prescreen potential subjects for eligibility.
  • Conduct psychometric rating scales for various diagnoses in clinical trials.
  • Ensure subject safety and respond to potential harm.
  • Calculate and utilize rating results to determine protocol eligibility.
  • Meet with Sponsors, Study Monitors, and Medical Monitors as needed.
  • Maintain consistency in ratings and review across studies.
  • Maintain source documentation per ALCOA-C standards and respond to queries.
  • Complete sponsor-required trainings and certifications for rater roles.
  • Attend company trainings and webinars as needed; maintain confidentiality per HIPAA.
  • Perform other duties as assigned.

Kenntnisse

MS Office
Typing 40 wpm
Organizational skills
Communication skills
Interpersonal skills
Multitasking
Professional conduct
HIPAA compliance

Ausbildung

Master’s degree

Tools

Electronic health records

Jobbeschreibung

Alcanza Clinical Research, LLC in Decatur, GA, seeks a Clinical Rater to interview participants for multi-site trials across ADHD, Alzheimer's, MDD and more, ensuring compliance with FDA, GCP and HIPAA.

The role emphasizes prescreening, administering standardized scales, documenting findings, and maintaining ALCOA-C source records, with opportunities for certification and professional growth.

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