2 часа назад
Clinical Trial Psych Rater - German Speaking
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trial Psych Rater - German Speaking (Psychiatric Clinical Assessments): Reviewing psychiatric assessment scales and clinical trial case data, conducting live rater discussions, and supporting standardized scoring with an accent on assessment methodology, documentation, and rater calibration. Focus on evaluating assessment quality, guiding raters through structured clinical interviews, and maintaining reliable clinical trial data.
Location: Remote/Virtual, associated with Berlin, Germany
Company
IQVIA provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for life sciences and healthcare organizations.
What you will do
- Complete orientation, training, calibration, and other required activities.
- Review clinical trial case data and prepare documentation for rater discussions.
- Conduct live discussions with raters about assessment methodology and scoring.
- Evaluate assessment quality and support rater performance through functional assessments and mock interviews.
- Submit accurate documentation and complete assigned interactions according to schedule.
Requirements
- Master’s degree in Psychology, Counseling, Psychiatric Nursing, Social Work, or an equivalent field.
- At least 3 years of experience administering psychiatric assessments, rating scales, or structured clinical interviews.
- At least 3 years of clinical experience with psychiatric populations and in clinical research trials.
- Experience with instruments such as MINI, MADRS, CAPS, PCL-5, C-SSRS, CGI, PANSS, AIMS, BARS, LSAS, or PGI-S.
- Native-level German and fluent English required.
- Strong communication, organization, attention to detail, time management, problem-solving, and Microsoft Office skills.
Nice to have
- MD, DO, or PhD.
- Experience in CNS clinical trials.
Culture & Benefits
- Remote/virtual part-time schedule.
- Estimated workload of 10–16 hours per month.
- Work supporting clinical trial data quality and standardized psychiatric assessments.
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