15 часов назад
Clinical Independent Rater for Clinical Trial - Mandarin Speaking
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Independent Rater for Clinical Trial - Mandarin Speaking (Psychiatric Assessments): Reviewing clinical trial rating scales and guiding raters through standardized assessment methodology with an accent on MINI, MADRS, psychiatric populations, and clinical research trials. Focus on evaluating assessment quality, conducting live rater discussions, supporting calibration, and completing accurate clinical documentation.
Location: Remote/Virtual; Singapore
Hours: 10–16 hours per month
Company
IQVIA provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for the life sciences and healthcare industries.
What you will do
- Participate in orientation, training, and calibration activities.
- Review case data and prepare documents and scale items for rater discussions.
- Conduct live interactions with raters to provide feedback on assessment methodology and scoring.
- Support rater performance through functional assessments, including 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.
- 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.
- Native-level Mandarin and fluent English are 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 trials.
Culture & Benefits
- Part-time remote/virtual engagement.
- Estimated workload of 10–16 hours per month.
- Work focused on improving the integrity and reliability of clinical trial data.
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