Study Start-Up Specialist II – Regulatory

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,...

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...

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...

Regulatory Affairs Study Start Up Specialist II (RASSU) Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. Prepare and QC Clinical Trial...

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) Join to apply for the Regulatory Affairs Study Start Up Specialist II (RASSU) role at CTI Clinical Trial and Consulting Services What You’ll Do Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. Handle regulatory submissions for medical devices, GMOs,...

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...

What you will be doing Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications. Coordinating and liaising with internal and external stakeholders to obtain necessary approvals and authorizations for study initiation. Managing and maintaining...

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...