9 дней назад
Clinical Trial Psych Rater - Slovak Speaking (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Trial Psych Rater - Slovak Speaking (Clinical Research): Reviewing psychiatric assessment scales and clinical trial case data, guiding raters on standardized methodology and scoring with an accent on PANSS, CGI-S, MADRS, and MINI. Focus on conducting live rater discussions, evaluating assessment quality, supporting calibration activities, and ensuring accurate clinical trial documentation.
Location: Remote/Virtual, with the role associated with Bratislava, Slovakia
Company
provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for the life sciences industry.
What you will do
- Participate in required orientation, training, and calibration activities.
- Review clinical trial case data and prepare documents and scale items for rater discussions.
- Conduct live interactions with raters to provide guidance on assessment methodology and scoring.
- Evaluate assessment quality and support rater performance through functional assessments such as mock interviews.
- Complete scheduled tasks and submit accurate documentation on time.
Requirements
- Master’s degree in Psychology, Counseling, Psychiatric Nursing, Social Work, or an equivalent field; MD, DO, or PhD preferred.
- At least 3 years of experience administering psychiatric assessments, rating scales, or structured clinical interviews, specifically PANSS, CGI-S, MADRS, and MINI.
- At least 3 years of clinical experience with psychiatric populations and at least 3 years administering scales in clinical research trials.
- Native-level Slovak and fluent English are required.
- Strong communication, organization, attention to detail, time management, and problem-solving skills.
- Proficiency with Windows and Microsoft Office applications.
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 arrangement.
- Work supporting clinical trial data integrity and standardized psychiatric assessments.
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