Remote Clinical Trial Rater — BPD Assessment Specialist

IQVIA Argentina

Philadelphia (Philadelphia County)

In loco

USD 13.000 - 17.000

Part-time

14 giorni+
Generatore di candidature

Distinguiti per questa posizione — genera un curriculum e una lettera di presentazione personalizzati in circa un minuto.

Supera i filtri ATS

Vantaggi offerti da questo lavoro

Remote work possibilities
Flexible schedule
Contract-based

Descrizione del lavoro

IQVIA is seeking a Clinical Trial Rater for a remote, part-time role focused on Borderline Personality Disorder assessments. You will conduct interviews, administer and score CGI scales, and maintain inter-rater reliability across multiple time points, ensuring data quality in accordance with GCP and protocol.

The role requires clinical judgment, psychiatric experience, and careful handling of safety issues while collaborating with study teams and sponsors. Immediate start, contract-based.

Competenze

  • Education and licensure as listed in qualifications.
  • 3+ years of clinical experience with BPD.
  • 3+ years of Clinical Trial Rater experience with semi-structured psychiatric assessments.

Mansioni

  • Conduct structured and semi-structured clinical interviews with trial participants.
  • Administer, score, and document CGI-S and CGI-C/CGIC-S ratings.
  • Maintain inter-rater reliability through calibration and quality reviews.
  • Identify safety concerns (e.g. suicidality) per protocol.
  • Collaborate with investigators, site staff, and sponsor/CRO teams.

Conoscenze

Clinical assessment
Inter-rater reliability
GCP knowledge
Trauma-informed approach

Formazione

PhD or PsyD / MD/DO
Licensure: MD/FMD/DO or licensed psychologist/psychiatrist

Strumenti

CGI-S
CGIC-S/CGI-C
Structured interviews

Descrizione del lavoro

IQVIA is seeking a Clinical Trial Rater for a remote, part-time role focused on Borderline Personality Disorder assessments. You will conduct interviews, administer and score CGI scales, and maintain inter-rater reliability across multiple time points, ensuring data quality in accordance with GCP and protocol.

The role requires clinical judgment, psychiatric experience, and careful handling of safety issues while collaborating with study teams and sponsors. Immediate start, contract-based.

Ottieni la revisione del curriculum gratis e riservata.

o trascina qui il file.

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