Site Partner II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Manager, Regulatory & Start Up – Sponsor Dedicated Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget
Team Introduction The Monetization Strategy & Operations team at TikTok LATAM plays a crucial role in driving strategic insights, optimizing performance, and enabling data-driven decision-making to fuel the region’s rapid growth. We are a high-performing, cross-functional
Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within
Job Overview: Primary contact with investigative site(s) during site start-up activities and maintenance with responsibility for collection of the required investigator and essential documents for a study, to ensure EC/IRB/Third body/Regulatory Authority and any other local applications are
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
The Clinical Study Administrator (CSA) assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality and consistency of interventional study deliverables to
At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech-tailored delivery model, we accelerate clinical development from early phase through global registrational
Study Start Up Manager Join Medpace as a full‐time, office‐based Regulatory Submissions Manager in Mexico City.This role plays a key part in the study start‐up process, building on your experience in clinical trials and regulatory submissions.You will use your expertise
ICON is a world-leading healthcare intelligence and clinical research organization seeking a Study Start Up Associate II.You will lead site initiation, ensure regulatory compliance, and contribute to advancing innovative therapies by coordinating regulatory submissions and stakeholder communications.You will
Study Start Up Associate II - Mexico - Homebased 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
Study Start-Up & Maintenance Senior Manager Category :Data & AI Location :Mexico City, Mexico City, MX Are you ready to transform clinical trial start-up timelines in one of the most complex regulatory environments? We are looking for a strategic
Prefer Clinical Regulatory Exp. 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
Study Start Up ManagerJoin Medpace as a full‐time, office‐based Regulatory Submissions Manager in Mexico City. This role plays a key part in the study start‐up process, building on your experience in clinical trials and regulatory submissions. You will use your
Study Start Up Associate I 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
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 in
Study Start Up Associate I - Hybrid - Mexico City 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
Job Advert Posting - 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