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東京都の臨床開発・薬事の求人231件

Clinical Research Coordinator

GEヘルスケア・ジャパン株式会社

この会社の求人 47件

掲載中・今日に確認

給与
記載なし
勤務地
東京都
休日
記載なし
雇用形態
記載なし

どんな仕事かAIによる生成

The Clinical Research Coordinator coordinates and manages in-house clinical research for the GE HealthCare Ultrasound business in Japan. The role works under the direction of the Global Research Team and closely with the local Principal Investigator and other study stakeholders. The role requires physical presence at the designated facility during volunteer research and ultrasound scanning sessions; ultrasound scanning is not a core responsibility.

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この求人に応募

給与記載なし

募集元で応募するGEヘルスケア・ジャパン株式会社の採用ページへ
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応募資格

必須

  • Bachelor’s degree in science, healthcare, engineering, a research-related field, or equivalent relevant experience.
  • Previous experience with a minimum of two years in clinical research or closely related research operations.
  • Outstanding organizational skills and meticulous attention to detail.
  • Proficiency with Microsoft Office applications, including Excel, Outlook, and Word.
  • Excellent Japanese communication skills for interaction with research volunteers and local study staff.
  • Strong business English skills, written and verbal, sufficient to communicate independently with the Global Research Team in routine virtual meetings and correspondence; explain study status, issues, risks and actions; prepare and review study documentation; and complete English-language GCP and internal procedure training.
  • Ability to manage multiple studies, participant schedules, documentation deliverables, and competing priorities with limited supervision.
  • Ability and willingness to work on-site during scheduled volunteer research and ultrasound scanning sessions.

歓迎

  • CCRC or CCRP certification preferred.
  • Previous experience as a Clinical Research Coordinator.
  • Experience with GCP-governed clinical research, IRB submissions, monitoring, audits, and study-document management.
  • Experience working in a global or cross-functional research organization.
  • Healthcare or medical-device experience, particularly in diagnostic ultrasound.
  • Hands-on ultrasound scanning experience is a plus, but is not required. Any scanning assignment is subject to study-specific restrictions, training, qualification, and delegation.
  • Ability to build effective working relationships across time zones and functions while maintaining clear ownership and follow-through.

募集要項最終確認 11/6

職種
臨床開発・薬事
雇用形態
記載なし
給与
記載なし
勤務地
東京都Hino
働き方
This role requires physical presence at the designated GE HealthCare facility during volunteer research and ultrasound scanning sessions.
経験年数
2年以上
学歴
大学卒業以上
掲載日
2026/11/05 16:11（1日前）
最終確認
2026/11/06 00:27（今日）

仕事内容

Job Description Summary

  • The Clinical Research Coordinator is responsible for coordinating and managing in-house clinical research for the GE HealthCare Ultrasound business in Japan.
  • The role works under the direction of the Global Research Team and works closely with the local Principal Investigator (PI), Research Program Integrators, study monitors, engineers, clinical specialists, and other study stakeholders.

Essential Responsibilities

  • Duties include (but are not limited to):
  • · Recruit, screen, enroll, and obtain informed consent from study participants.
  • · Coordinate and oversee research sessions, including scheduling participants, reserving space, ensuring staff training, and managing documentation.
  • · Ensure compliance with the study protocol, applicable regulations, GCP and IRB requirements, and internal GE HealthCare processes.
  • · Maintain study documentation, including regulatory binders, source documentation, trackers, training records, delegation records, and other study materials.
  • · Complete and coordinate IRB submissions and correspondence, including new submissions, continuing review or renewal, amendments, deviation reports, adverse event reports, and other required notifications.
  • · Conduct training and provide guidance to study staff.
  • · Facilitate monitoring visits, respond to document requests and follow-up actions, and prepare for audits as needed.
  • · Serve as the main operational point of contact for research volunteers and study staff.
  • · Maintain research facilities, including the consent area and scan bays; order supplies and track spend.
  • · Implement process improvements and electronic processes to facilitate compliance, traceability, data integrity, and efficiency.
  • · Provide support to Research Program Integrators and other study stakeholders as needed.
  • · Serve as a Subject Matter Expert for coordinators at global sites executing similar protocols.
  • · Coordinate routinely with the Global Research Team through written communication and virtual meetings; communicate study status, issues and risks; and follow up on agreed actions.
  • · Identify and promptly escalate protocol deviations, participant concerns, documentation gaps, data-quality issues, and other study risks to the PI and appropriate global study stakeholders.
  • · Ultrasound scanning is not a core responsibility. Depending on study needs, applicable restrictions, documented training and qualification, and formal delegation, the employee may support limited protocol-driven ultrasound data collection.
  • This role requires physical presence at the designated GE HealthCare facility during volunteer research and ultrasound scanning sessions.

この求人は、GEヘルスケア・ジャパン株式会社の採用ページの内容をAIが読み取って整理したものです。応募の前に採用ページの原文を確かめてください。データの集め方企業サイト

同じ会社の求人47件

GEヘルスケア・ジャパン株式会社の求人をすべて見る（47件）

職種と勤務地が似ている求人東京都の臨床開発・薬事 231件

東京都の臨床開発・薬事の求人をすべて見る（231件）

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