1 день назад
Clinical Trial Psych Rater - Mandarin Speaking
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Trial Psych Rater - Mandarin Speaking (Psychiatric Clinical Trials): Reviewing psychiatric assessment scales and clinical trial case data with an accent on standardized methodology, scoring accuracy, and rater performance. Focus on conducting live feedback discussions, evaluating MINI and MADRS assessments, and completing calibration and documentation activities.
Location: Remote/Virtual, with the role listed in Beijing, China; estimated 10–16 hours per month
Company
Provides clinical research services, healthcare intelligence, analytics, and technology solutions for pharmaceutical, biotechnology, and medical device organizations.
What you will do
- Complete required orientation, training, and calibration activities.
- Review case data, relevant documents, and scale items before rater discussions.
- Conduct live discussions 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 assigned interactions and submit accurate documentation on 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, specifically MINI and MADRS.
- At least 3 years of clinical experience with psychiatric populations.
- At least 3 years of experience administering scales in clinical research trials, excluding graduate or doctoral research.
- Fluent English and native-level Mandarin proficiency 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
- Part-time remote/virtual work.
- Estimated workload of 10–16 hours per month.
- Structured training, calibration, and scheduled rater interactions.
- Work supporting the integrity and reliability of clinical trial data.
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