Global Site Start-Up

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 the study start up process at Medpace.If you want an exciting career where you use your previous expertise and can...

Clincal Development CenterMéxicoAre you passionate about clinical trial management and regulatory excellence Do you thrive in an unordinary and dynamic environment where collaboration and innovation drive success If you have a strong background in clinical development and are ready to lead the way in ensuring seamless trial start-up activities we want to...

A global healthcare research organization is seeking a Study Start Up Associate I in Mexico City.The position involves facilitating clinical trial initiation, ensuring compliance and managing site communications.Ideal candidates will hold a Bachelor's degree in life sciences and possess strong organizational, communication, and multitasking abilities.The...

Study Start Up Associate II (Site Activation Associate) - Mexico - HomebasedICON 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 future of clinical developmentAt ICON, it's our people...

Study Start Up Associate II - Mexico - HomebasedICON 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 future of clinical developmentWe are currently seeking a Study Start Up Associate II...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.May also include maintenance activities.Essential Functions- Under general supervision, serve as...

A leading clinical research organization in Mexico City is seeking a Regulatory Submissions Manager to oversee the start-up process for clinical trials.Candidates should have at least 4 years of relevant experience with strong communication and leadership skills.The role is office-based with a focus on managing global start-up activities and ensuring the...

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 improve patients' lives.- ICON plc is a world-leading healthcare intelligence and clinical research organization.From molecule to medicine, we advance clinical research by...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.May also include maintenance activities.Essential Functions- Under general supervision, serve as...

Senior Site Partner - Hybrid - Mexico CityICON 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 future of clinical developmentWe are currently seeking a Senior Site Partner to join our...