Bio
Our professionals apply their therapeutic, regulatory, and operational expertise to consistently solve the challenges that arise during clinical projects.
Members of our Study Start Up team are focused on clinical trial site activation and efficient study start-up for both site-based and remote/de-centralized trials are critical to drug development programs, in terms of time, cost and quality of data.
Please find other roles I support in the Americas region below as we are always looking for great talent to join our ICON family!
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Life at ICON
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IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
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Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
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Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
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