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1 день назад

Clinical Independent Rater for Clinical Trial - Turkish Speaking

Формат работы
remote (только Turkey)
Тип работы
parttime
Английский
c1
Страна
Turkey
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Independent Rater for Clinical Trial - Turkish Speaking (psychiatric clinical assessments): Reviewing clinical trial assessments and conducting patient interviews with an accent on standardized rating scales, structured interviews, and protocol compliance. Focus on administering and interpreting MINI and MADRS, guiding raters through live discussions, and maintaining reliable clinical trial data.

Location: Remote/Virtual; position listed in Istanbul, Turkey

Company

Global provider of clinical research services, healthcare intelligence, advanced analytics, and technology solutions for life sciences and healthcare organizations.

What you will do

  • Complete required orientation, training, and calibration activities.
  • Review case data and prepare documents and assessment materials for rater discussions.
  • Conduct patient interviews and clinical assessments with study participants.
  • Administer, score, and interpret clinical rating scales and structured interviews.
  • Provide live feedback and guidance to raters on methodology, interview techniques, and scoring accuracy.
  • Submit assessment records, reports, and documentation accurately within study timelines.

Requirements

  • Master’s degree in Psychology, Counseling, Psychiatric Nursing, Social Work, or an equivalent qualification; MD, DO, or PhD is preferred.
  • At least 3 years of experience administering psychiatric assessments, rating scales, and 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.
  • Fluency in English and native-level Turkish proficiency required.
  • Strong communication, organization, attention to detail, time management, problem-solving, and Microsoft Office skills.

Nice to have

  • Experience in CNS clinical trials.
  • MD, DO, or PhD qualification.

Culture & Benefits

  • Remote/virtual work arrangement.
  • Estimated workload of 10–16 hours per month.
  • Work supporting clinical trial data quality, standardized assessments, and patient outcomes.

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