Site Engagement Manager

Senior CRA (UCB SEM)

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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

ICONにおけるシニアCRAとして、エンゲージﾒﾝﾄのマネジメントの業務を担当していただく想定です。医療機関・治験責任医師との関係性を通じて臨床試験の成功を支えていただく重要なポジションです。

応募資格

• ライフサイエンス、看護学、医学など関連分野における学士号以上
• CRAとしての豊富な実務経験および臨床試験プロセス・規制要件に関する深い理解
• 複数の施設・プロジェクトを同時に管理できる高い調整力および問題解決能力
• モニタリング業務、データ品質管理、施設管理に関する専門知識、および臨床試験関連システムの使用経験
• 優れたコミュニケーション力・対人折衝力を有し、複雑な環境下でも関係者を巻き込みコンプライアンスを推進できる方
• 国内外への出張が可能な方（目安：稼働時間の60%以上）および有効な運転免許をお持ちの方

What ICON can offer you:

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.

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