Home Based - Regulatory Exp.- CDMX 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,
Are you ready to transform clinical trial start-up timelines in one of the most complex regulatory environments? We are looking for a strategic and hands-on leader who can challenge the status quo, optimize processes, and drive faster,
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
Link-Worldwide in Mexico City is seeking a member for the Study Start Up Team. You will ensure physicians at research sites are ready to start clinical trials of investigational products. Ideal candidates have a Bachelors Degree in Life Sciences
Purpose :The Specialist, Country SSU proactively drives and executes all start up and maintenance related activities and deliverables for assigned studies and sites in their assigned country or countries. - Note: Specialists will report into their local country
Regulatory Exp. Home Based - CDMX ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on
Link-Worldwide is seeking a Study Start Up Associate with experience in reviewing Informed Consent Forms to ensure readiness for clinical trials. The role involves significant collaboration with stakeholders, including sponsors and legal teams, to negotiate and finalize ICF
Job SummaryJoin 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 up! You will be
A clinical research organization in Mexico City is seeking a Regulatory Submissions Coordinator to support Regulatory Submissions and gain vital experience in study start-up. Responsibilities include providing support activities, ensuring compliance, and conducting document quality control. Requirements include
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
Link-Worldwide is seeking a candidate for a role focused on managing contracts and budgets for clinical site investigations in Valle de Chalco Solidaridad, Estado de México. The successful candidate will be responsible for negotiating contracts, preparing
As a Study Start Up Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing : - Manages start-up activities for assigned studies at the regional level
PositionAs a key member of the Country Study Start-Up Team, you will play a crucial role in delivering clinical trials to patients by driving and facilitating efficient study start-up processes.ResponsibilitiesCreating and executing effective strategies for trial initiation.Managing and ensuring timely
The Study Start Up.Assocate II, collect, prepare, review, approve, process and track regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable country regulations/guidelines and the principles of ICH/GCP. -
At ICON, its our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives.Our Own It
Link-Worldwide is seeking a Study Start Up Associate I to support the initiation of clinical trials in Mexico City. The role involves coordinating with stakeholders for study approvals and maintaining regulatory compliance, ensuring the quality of work. Candidates should
Summary Monitors patient data and study-related information related to clinical study sites and clinical trial participation. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into data validation plan. Provides timely
Link-Worldwide is seeking a vendor management specialist in Ciudad de México. The role includes performing various FSA activities, maintaining tracking systems, and mentoring junior team members. Candidates should have at least two years of experience with
Link-Worldwide is seeking a talented member of the Country Study Start-Up Team to deliver clinical trials efficiently. You will be responsible for managing site activation, ensuring regulatory compliance, and creating strategies for trial initiation.The ideal candidate has a
About the Role At ICON, its 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