Medical Device Clinical Start-Up Specialist II

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...

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...

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...

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...

A leading clinical research organization is seeking a Study Start Up Associate II to manage clinical trial site start-up activities. This role involves coordinating regulatory submissions, collecting essential documentation, and fostering relationships with clinical sites. The ideal candidate should have a Bachelor's degree, 2+ years in clinical research,...

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,...

A leading clinical research organization in Madrid is seeking a Site Start-Up Specialist to coordinate site start-up activities and manage regulatory submissions. In this role, you will ensure compliance with ICH/GCP guidelines and collaborate with stakeholders to advance innovative treatments. Applicants should have at least 2 years of clinical research...

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...