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Senior Global Regulatory Scientist
ICON Clinical Research
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Mexico City, Mexico
Location
Mexico City
Posted
June 15, 2026
Commute
Local Area
Local Opportunity Near You!
This job is in your area. Enjoy a short commute and work close to home.
Job Description
Homebased role
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre 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 Global Regulatory Scientist to join our diverse and dynamic team. As a Senior Global Regulatory Scientist at ICON, you will provide high-level regulatory and scientific expertise to support global development strategies and submissions. You will collaborate with sponsors and cross-functional teams to navigate complex regulatory pathways and enable successful product development.
**What You Will Be Doing:**
+ Leading the development of global regulatory strategies for clinical programmes, including plans for key health authority interactions and milestones.
+ Authoring and reviewing complex regulatory documents such as clinical trial application...
ICON plc is a world-leading healthcare intelligence and clinical research organization. Weβre 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 Global Regulatory Scientist to join our diverse and dynamic team. As a Senior Global Regulatory Scientist at ICON, you will provide high-level regulatory and scientific expertise to support global development strategies and submissions. You will collaborate with sponsors and cross-functional teams to navigate complex regulatory pathways and enable successful product development.
**What You Will Be Doing:**
+ Leading the development of global regulatory strategies for clinical programmes, including plans for key health authority interactions and milestones.
+ Authoring and reviewing complex regulatory documents such as clinical trial application...