Clinical Trial Manager

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

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

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

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

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

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

Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland.

iconplc.com