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Clinical Independent Rater for Clinical Trial (CIR) – Japanese Speaking
給与
記載なし※ 募集要項に金額の記載がありません
- 勤務地
- 東京都
- 雇用形態
- 記載なし
- 働き方
- 国内フルリモート可
- 年間休日
- 記載なし
フルリモート
要約求人票をもとにAIがまとめたものです
Conducts remote clinical interviews and psychiatric assessments for participants in an ongoing CNS clinical research study. The role administers standardized PTSD-related rating scales and structured interviews, and supports protocol compliance, data quality, and participant safety.
応募資格
必須
- Master's degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, Social Work, or a related clinical discipline.
- Minimum 2 years of clinical experience with PTSD populations.
- Minimum 2 years of experience administering CAPS-5 and/or other structured psychiatric interviews.
- Strong understanding of PTSD diagnosis, symptomatology, and treatment.
- Demonstrated competency administering structured clinical interviews and rating scales.
- Excellent verbal and written communication skills.
- Strong attention to detail and commitment to assessment quality and consistency.
- Effective organizational and time-management skills.
- Ability to work independently in a remote environment.
- Proficiency with Microsoft Office applications and web-based clinical platforms.
- Current openings require fluency in English and native-level proficiency in Japanese.
- Candidates must be able to conduct clinical interviews and complete all study-related communications in both English and the required language.
歓迎
- PhD, PsyD, MD, DO, or equivalent advanced clinical qualification preferred.
- Completion of all four CAPS-5 certification modules/certificates preferred.
- Experience administering psychiatric assessments within clinical research trials.
- Experience with CNS and/or psychiatric clinical studies.
- Experience conducting remote or centralized assessments.
- Familiarity with PTSD outcome measures and structured diagnostic interviews.
- Previous experience serving as an independent rater, interviewer, or clinical trial assessor.
- CAPS-5 Certification (all four certificates preferred)
- Good Clinical Practice (GCP) Training
- Other relevant structured interview certifications and psychiatric rating scale training
使用ツール
募集要項最終確認 9/26
- 職種
- 応用研究員
- 雇用形態
- 記載なし
- 給与
- 記載なし
- 勤務地
- Tokyo, Japan
- 働き方
- **Location:** Remote/VirtualConduct protocol-required remote clinical interviews and assessments with study participants.
- 勤務時間
- **Hours:** Estimated 10–16 hours per month
- 経験年数
- 2年以上
- 学歴
- 大学院修了以上
- 掲載日
- 2026/09/24 00:55（5日前）
- 最終確認
- 2026/09/26 01:25（3日前）
仕事内容
Position Overview
IQVIA is seeking experienced Clinical Interview Raters (CIRs) with expertise in Post-Traumatic Stress Disorder (PTSD) for an ongoing CNS clinical research study.
This role is responsible for conducting standardized clinical interviews and psychiatric assessments with study participants, ensuring protocol compliance, data quality, and consistency across all evaluations.
Assessments utilized in this study include:
MINI International Neuropsychiatric Interview (MINI)
Montgomery-Åsberg Depression Rating Scale (MADRS)
Clinician-Administered PTSD Scale for DSM-5 (CAPS-5)
PTSD Checklist for DSM-5 (PCL-5)
Columbia Suicide Severity Rating Scale (C-SSRS)
Clinical Global Impression – Severity for PTSD (CGI-S-PTSD)
Clinical Global Impression – Change for PTSD (CGI-C-PTSD)
Key Responsibilities
Conduct protocol-required remote clinical interviews and assessments with study participants.
Administer and score study-specific psychiatric rating scales and structured interviews according to sponsor and protocol requirements.
Maintain consistency and reliability across all participant assessments.
Participate in study training, calibration, standardization, and certification activities as required.
Review participant history and relevant documentation prior to assessments.
Complete assessments, documentation, and data entry within required timelines.
Ensure compliance with Good Clinical Practice (GCP), study protocols, and applicable regulations.
Collaborate with clinical teams and study stakeholders to support data quality and participant safety.
Attend project meetings and ongoing quality review sessions when required.
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