2 часа назад
Clinical Trial Psych Rater - Hungarian Speaking
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trial Psych Rater - Hungarian Speaking (Psychiatric Clinical Research): Reviewing psychiatric assessment scales and clinical trial case data with an accent on standardized methodology, scoring accuracy, and rater calibration. Focus on conducting live rater discussions, evaluating assessment quality, and supporting structured clinical interviews using SCID-5, PANSS, and CGI.
Location: Remote/Virtual; Budapest, Hungary
Company
provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for the life sciences and healthcare industries.
What you will do
- Complete required orientation, training, and calibration activities.
- Review case data and prepare documentation for discussions with clinical trial raters.
- Conduct live interactions with raters, providing guidance on assessment methodology and scoring.
- Support rater performance through functional assessments such as mock interviews.
- Complete assigned tasks and submit accurate documentation on schedule.
Requirements
- Master’s degree in Psychology, Counseling, Psychiatric Nursing, Social Work, or an equivalent field; MD, DO, or PhD is preferred.
- At least 3 years of experience administering psychiatric assessments, rating scales, or structured clinical interviews, specifically SCID-5, PANSS, and CGI.
- At least 3 years of clinical experience working with psychiatric populations.
- At least 3 years of experience administering scales in clinical research trials, excluding graduate or doctoral research.
- Native-level Hungarian proficiency and fluent English are required.
- Strong communication, interpersonal, organizational, time-management, attention-to-detail, and problem-solving skills, plus proficiency with Windows and Microsoft Office.
Nice to have
- MD, DO, or PhD.
- Experience in CNS clinical trials.
Culture & Benefits
- Part-time schedule of approximately 10–16 hours per month.
- Remote/virtual work format.
- Work supporting clinical trial data integrity and improved patient outcomes.
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