Clinical Psychometric Rater - Trials & Assessments

Alcanza Clinical Research, LLC

Decatur (GA)

Vor Ort

USD 55.000 - 75.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Health, dental, vision insurance
401k with safe harbor match
Disability insurance

Zusammenfassung

Alcanza Clinical Research, LLC in Decatur, GA is seeking a Clinical Rater to interview participants and informants for health studies, ensuring compliance with study protocols, SOPs, GCP, ICH and FDA regulations.

The role requires a Master’s degree and 1+ year experience with psychometric rating scales; candidates should have strong communication, meticulous documentation, and the ability to work independently within a team.

Qualifikationen

  • Master’s degree and 1+ year experience in psychometric rating scales in clinical settings or trials.
  • Certifications to rate scales (SCID-5-CT, MINI, HAM-A/D, PANSS, etc.) are preferred.
  • Bi-lingual English/Spanish proficiency is a plus; BLS is preferred.

Aufgaben

  • Review subject medical history and prescreen eligibility with study team input.
  • Conduct psychometric ratings across diagnoses (ADHD, Alzheimer’s, etc.).
  • Ensure safety by addressing potential harm per protocol and privacy rules.
  • Maintain ALCOA-C source documentation and respond to sponsor queries.
  • Complete trainings to obtain and renew rater certification.

Kenntnisse

Psychometric rating scales
Clinical trials experience
HIPAA compliance
Data entry / EHRs
Communication skills
Attention to detail
Bilingual English/Spanish

Ausbildung

Master’s degree
1+ year psychometric rating experience

Tools

Microsoft Office
Electronic health records
Web applications

Jobbeschreibung

Alcanza Clinical Research, LLC in Decatur, GA is seeking a Clinical Rater to interview participants and informants for health studies, ensuring compliance with study protocols, SOPs, GCP, ICH and FDA regulations.

The role requires a Master’s degree and 1+ year experience with psychometric rating scales; candidates should have strong communication, meticulous documentation, and the ability to work independently within a team.

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