Medical Device Study Start-Up Specialist II

A global clinical research organization is seeking a Study Start Up Associate II in Madrid. The role involves coordinating site regulatory submissions and ensuring compliance with legal standards. Ideal candidates will have a Bachelor’s degree and 2+ years of experience in clinical research. Responsibilities include document collection, partnering with...

Overview Study Start Up Associate II - Medical Device - Arden Hills, MN 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 future of clinical development. Through coordination with...

OverviewStudy Start Up Associate - Arden Hills, MNICON 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 development.What you will be doingThrough coordination with...

Overview Study Start Up Associate - Arden Hills, MN 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 future of clinical development. What you will be doing Through...

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...

Regulatory Affairs Study Start Up Specialist II (RASSU)Dé el siguiente paso en su carrera profesional ahora: desplácese hacia abajo para leer la descripción completa del puesto y envíe su solicitud.Join to apply for theRegulatory Affairs Study Start Up Specialist II (RASSU)role atCTI Clinical Trial and Consulting ServicesWhat You’ll DoPrepare, review,...

Study Start Up Associate II - ICF 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 future of clinical development Study Start Up Associate (Informed Consent) We are looking for...

A leading healthcare research organization is seeking a Study Start Up Associate to coordinate activities for regulatory submissions and manage essential documents for clinical trials. The ideal candidate will have a Bachelor's degree and at least 2 years of experience in clinical research, particularly in site start-up processes. This role involves working...

A leading healthcare research organization is seeking a Study Start Up Associate to coordinate activities for regulatory submissions and manage essential documents for clinical trials. The ideal candidate will have a Bachelor's degree and at least 2 years of experience in clinical research, particularly in site start-up processes. This role involves working...

Regulatory Affairs Study Start Up Specialist II (RASSU)Todos los candidatos deben asegurarse de leer atentamente la siguiente descripción del puesto y la información antes de enviar su solicitud.Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS.Handle regulatory submissions for medical devices, GMOs, and...