buscando un a Study Advisor para unirse al equipo en la oficina de Ciudad de México. En el equipo de B2B Brasil trabajan directamente... con los estudiantes de empresas que contratan cursos de idiomas para sus colaboradores. Como Study Advisor, la labor principal es brindar...
, even when the original vendor no longer provides support. This is a hands-on, engineering-heavy role. You will not just study...
. We offer an appealing working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance...
of experience in the same position. Bachelor’s degree required;completed degree preferred. Preferred fields of study...
Study Start Up Associate II (Investigator Pricing Analyst/ Budget Analyst) ICON is a global healthcare intelligence... in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research. We are seeking a , Study...
**SUMMARY**:**The Study Coordinator (SC) successfully supports the site's Principal Investigator (PI) in the... and coordinate the daily clinical research study/studies activities and play a critical role in the conduct of the study. The SC...
Study Start Up Associate II (Investigator Pricing Analyst/ Budget Analyst) ICON plc is a world-leading healthcare... in clinical research . We are seeking a , Study Start Up Associate II ( Investigator Pricing Analyst/ Budget Analyst...
Lugar:
Veracruz, Ver. | 23/08/2026 17:08:37 PM | Salario: S/. No Especificado | Empresa:
ICON, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Study Start Up... and authorizations for study initiation. Maintaining accurate and up-to-date records of regulatory submissions and approvals...
, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study...: Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good...
, you will support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study...: Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good...