9 дней назад
Clinical Independent Rater - Romanian Speaker (Clinical Trials)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Independent Rater - Romanian Speaker (Clinical Trials): Reviewing clinical trial assessments and conducting participant interviews with an accent on psychiatric rating scales, structured clinical interviews, and protocol-compliant data quality. Focus on administering and interpreting PANSS and SCID, guiding raters through live feedback, and completing accurate clinical documentation on schedule.
Location: Remote/Virtual; role listed in Bucuresti, Romania
Company
provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for the life sciences industry.
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 other documentation accurately and on schedule.
Requirements
- Master’s degree in Psychology, Counseling, Psychiatric Nursing, Social Work, or an equivalent field; MD, DO, or PhD is preferred.
- At least 3 years of experience administering psychiatric assessments, rating scales, or structured clinical interviews, specifically PANSS and SCID.
- At least 3 years of clinical trial experience with psychiatric populations and administering scales in clinical research trials.
- Strong interpersonal, communication, organizational, problem-solving, and time-management skills.
- Proficiency with Windows and Microsoft Office applications.
- Fluent English and native-level Romanian proficiency are required.
Nice to have
- MD, DO, or PhD degree.
- Experience in CNS trials.
Culture & Benefits
- Part-time schedule with an estimated workload of 10–16 hours per month.
- Remote/virtual work arrangement.
- Work focused on clinical trial data integrity, participant assessments, and patient outcomes.
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