Job Summary: Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based **Regulatory Submissions Manager** to join our Study Start Up team in Meixco City! This position plays a key role...
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfill our mission to advance and improve patients' lives. ICON plc is a world-leading healthcare intellig...
Job Summary: Join Medpace in Mexico! As a **Regulatory Submissions Coordinator** you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up! You will b...
About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey...
About the Role We are looking for a PO FollowUp Analyst to join our Procurement Shared Services PSS team. This is a newly created role that plays a key part in ensuring accurate purchase order status, supplier followup, and seamless commu...
Regulatory Exp.- Home Based - CDMX 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 ...
Regulatory & Start Up Specialist, cFSP. Location: Mexico - Full home based Job Overview This position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact ...
CDMX 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 futur...
Job Summary : Join Medpace at our Mexico City offfice! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start u...
Job Summary : Our LATAM clinical trial activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Manager to join our Study Start Up team in Mexico City! This position plays a key role in...