Назад
Company hidden
15 часов назад

Clinical Independent Rater for Clinical Trial - Mandarin Speaking

Формат работы
remote (только Singapore)
Тип работы
parttime
Грейд
middle
Английский
b2
Страна
Singapore
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

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.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →