Clinical Study Manager

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 experienced Clinical Trial Manager to join our diverse and dynamic team. As a Clinical Trial Manager, you will support the delivery of medical device clinical studies across Africa, the Middle East (including Israel), and India. This is a high-impact opportunity to work across diverse and growing regions, contributing to the advancement of innovative healthcare technologies.As Clinical Study Manager, you will take ownership of the operational delivery of medical device clinical studies, ensuring quality, compliance, and timelines are consistently achieved. You will act as a key interface between internal teams, CRO partners, and external stakeholders, driving studies from planning through to execution and close-out.

What you will be doing

• Lead the end-to-end management of medical device clinical studies across multiple regions
• Oversee study timelines, deliverables, and budgets, ensuring operational excellence
• Collaborate with and manage CRO partners to ensure effective study execution
• Contribute to protocol development, including defining study endpoints and methodology
• Ensure compliance with applicable regulatory requirements, with a strong focus on medical device regulations
• Manage submissions to ethics committees and relevant regulatory bodies
• Oversee study documentation, including Trial Master File quality and end of study reports
• Provide regional oversight across Africa and India, including on-site engagement as required

Your profile

• Bachelor's degree in a relevant field, with a minimum of 3 years of experience in clinical trial management.
• Prior experience as a Clinical Research Associate, combined with demonstrated project management experience
• Proven experience managing medical device clinical studies from start-up through close-out
• Strong understanding of medical device regulatory requirements and submission processes
• Experience working with CROs and managing external vendors
• Hands-on experience writing or contributing to clinical study protocols and endpoints
• Track record of submitting to ethics committees and preparing end of study documentation
• Experience working across Africa and or India regions is highly desirable
• Willingness and ability to travel extensively within the region
• Effective communication and interpersonal skills, with the ability to collaborate across diverse teams.
• Detail-oriented and organized, with a track record of successfully managing multiple tasks and priorities simultaneously.

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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