Question
FULL_TIME
0-2

IHCRA

12/2/2025

The IHCRA will assist in the planning, initiation, and execution of clinical trial activities, ensuring compliance with study protocols and regulatory requirements. This role involves monitoring study progress and data collection activities to maintain quality and accuracy.

Working Hours

40 hours/week

Company Size

10,001+ employees

Language

English

Visa Sponsorship

No

About The Company
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
About the Role
IHCRA, Full time, Japan

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and management of clinical trials, contributing to the advancement of innovative treatments and therapies.

What you will be doing

  • Assisting in the planning, initiation, and execution of clinical trial activities
  • Conducting site feasibility assessments and participating in site selection processes
  • Coordinating with investigative sites to ensure compliance with study protocols and regulatory requirements
  • Monitoring study progress and data collection activities to ensure quality and accuracy
  • Assisting in the preparation and review of study documentation and reports

Your profile

  • Bachelor's degree in a relevant field, such as life sciences or healthcare
  • Previous experience in clinical research or a related field preferred
  • Strong organizational and communication skills
  • Ability to work independently and collaboratively in a fast-paced environment
  • Attention to detail and ability to prioritize tasks effectively


現在、ICONでは多様でダイナミックなチームに加わる IHCRAを募集しています。IHCRAとして、臨床試験の実施と管理をサポートし、革新的な治療法や療法の発展に貢献する重要な役割を担っていただきます。

主な業務内容
・臨床試験活動の計画、開始、実施を支援
・治験施設の実施可能性評価を行い、施設選定プロセスに参加
・治験施設と連携し、試験プロトコルや規制要件の遵守を確保
・試験の進捗状況やデータ収集活動をモニタリングし、品質と正確性を担保
・試験関連文書や報告書の作成・レビューを支援

応募資格
・ライフサイエンスやヘルスケアなど関連分野の学士号
・臨床開発または関連分野での経験があれば尚可

・優れた組織力とコミュニケーション能力
・迅速な環境で自律的かつ協働的に業務を遂行できる能力
・細部への注意力と効果的な優先順位付けスキル

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements

  • A range of health insurance offerings to suit you and your family’s needs.

  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.

  • Life assurance

  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please click here to apply

Key Skills
Clinical ResearchSite Feasibility AssessmentStudy Protocol ComplianceData Collection MonitoringDocumentation PreparationCommunication SkillsOrganizational SkillsAttention to Detail
Categories
HealthcareScience & Research
Benefits
Annual LeaveHealth InsuranceRetirement PlanningEmployee Assistance ProgrammeLife AssuranceFlexible Benefits
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