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Clinical Trial Manager

  1. Osaka, Tokyo
JR148241
  1. ICON Full Service & Corporate Support
  2. Clinical Trial Management
  3. Hybrid

About the role

Clinical Trial Manager, 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 a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials, ensuring adherence to timelines, budgets, and regulatory guidelines. As a leader in our research department, you will collaborate with cross-functional teams, manage site relationships, and provide strategic guidance to drive the successful delivery of clinical trial outcomes.

What you will be doing

  • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
  • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
  • Build and manage strong relationships with trial investigators and stakeholders.
  • Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
  • Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile

  • University degree in medicine, science, or equivalent combination of education & experience
  • Demonstrated ability to drive the clinical deliverables of a study
  • Subject matter expertise in the designated therapeutic area
  • Prior monitoring experience is preferred
  • Ability to travel up to 20%

ICON Plc では現在、多様でダイナミックなチームの一員として Clinical Trial Manager を募集しています。
本ポジションでは、臨床試験の計画、実施、完了までの全プロセスを統括し、タイムライン、予算、規制ガイドラインを遵守しながら成功に導く重要な役割を担います。リサーチ部門のリーダーとして、部門横断的なチームと連携し、サイトとの関係構築を行い、臨床試験を成功裡に遂行するための戦略的な指導を提供していただきます。

■主な業務内容

・臨床試験のすべての側面を計画・管理し、タイムライン、予算、品質基準を順守する。
・臨床試験のプロトコルおよび手順の策定・実施に向けて、部門横断的チームと協働する。
・試験責任医師および関連ステークホルダーとの強固な関係を構築・維持する。
・すべての臨床試験が、各地域・国内・国際的な規制および倫理ガイドラインに従って実施されるよう確保する。
・試験デザイン、ベンダー選定、リスクマネジメントに関する重要な意思決定および課題解決を行う。


■求める人物像(Your Profile)

・医学、科学、または同等の教育・経験を持つ大学卒資格
・試験の臨床成果物をリードした実績
・指定された治療領域における専門性
・モニタリング経験があれば尚可
・最大 20% の出張が可能であること

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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized 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

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