Clinical Trial Assistant – Sponsor Dedicated Role

About the role

Sponsor Dedicated – FSP at ICON Strategic Solutions, you will work in a sponsor‑dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to treatments that benefit patients worldwide.

Key responsibilities

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Support the preparation of study‑related materials, such as informed consent forms and case report forms.
• Work with cross‑functional teams to facilitate communication and ensure smooth trial execution.
• Contribute to the tracking and reporting of clinical trial metrics and milestones.

Required profile

• Relevant clinical research experience.
• Bachelor’s degree in a scientific or healthcare‑related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills.
• Ability to work collaboratively in a fast‑paced environment with attention to detail.
• Willingness to travel as required (approximately 10%).

What we offer

• Competitive salary and a range of additional benefits focused on well‑being and work‑life balance.
• Various annual leave entitlements.
• Health insurance offerings for you and your family.
• Competitive retirement planning options.
• Global Employee Assistance Programme (LifeWorks) with 24‑hour access to professional support.
• Life assurance and flexible country‑specific optional benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, etc.