Remote Dutch-Speaking Clinical Rater (10–16 hrs/mo)

IQVIA; Utrecht; A distancia; EUR 69.000 - 110.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Clinical Independent Rater – Dutch Speaking. This remote/virtual role demands approximately 10–16 hours per month and focuses on reviewing scales, guiding raters on methodology, and supporting data integrity in clinical trials.

You will participate in training, calibrations, and live feedback sessions, working with rater teams across CNS trials. Fluent English and native-level US Dutch are required.

Formación

• Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
• Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (MINI and MADRS).
• Minimum 3 years of clinical experience with psychiatric populations.
• Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
• Experience in CNS trials preferred.

Responsabilidades

• Participate in all required orientation, training, and calibration activities.
• Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
• Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
• Complete assigned tasks and rater interactions according to schedule.
• Submit all required documentation accurately and on time.

Conocimientos

Interpersonal skills

Communication skills

Time management

Dutch proficiency

English fluency

Detail oriented

Windows

Educación

Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work

MD/DO/PhD preferred

Herramientas

Windows

Microsoft Office

Descripción del empleo

IQVIA is seeking a Clinical Independent Rater – Dutch Speaking. This remote/virtual role demands approximately 10–16 hours per month and focuses on reviewing scales, guiding raters on methodology, and supporting data integrity in clinical trials.

You will participate in training, calibrations, and live feedback sessions, working with rater teams across CNS trials. Fluent English and native-level US Dutch are required.