Start-Up Regulatory Associate II

Clinical Research Associate II / Senior Clinical Research (CRA) - ItalyJob Category: Clinical MonitoringRequisition Number: CLINI002065Posted : October 1, 2026Full-TimeRemoteLocationsShowing 1 locationItaly - RemoteDescriptionWhatYou'llDo:Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim...

Description Are you ready to grow with the world’s largest law firm? Join Dentons Italy Team today. Dentons Italy is currently looking to grow its Public Law and Regulatory group with the appointment of an Associate based in our Milan office. Our Public Law and Regulatory Team consists of specialized lawyers in the sector, recognized among the best for...

PSI is seeking a regulatory submissions specialist in the Milan area to facilitate start-up activities for clinical studies under the EU CTR framework. The role involves coordinating Italy CTR Part II submissions, communicating with authorities, project teams and vendors, and ensuring accurate document translations. The candidate should have a scientific...

Allucent seeks a Start-Up Associate II (SUA II) in Italy to coordinate local site start-up activities for clinical trials. You will manage regulatory submissions, maintain essential documents, and liaise with RA/IEC/IRB and investigators during the initial phase of studies.You will ensure compliance with local regulations, support ethical documentation, and...

Updated: Yesterday Location: Remote, I, Greece Job ID:25113642 Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate...

Overview Join Allucent as a Start-Up Associate II to lead local site start-up activities for clinical trials. You will coordinate regulatory and ethics submissions and serve as the primary point of contact with authorities, investigators, and sites through the initial study phase. You will manage documentation, timelines, and country-specific requirements to...

RA Principal Associate (M/F/X) Tasks: * Lead and execute regulatory strategies for assigned products and projects. * Prepare, compile, and submit high-quality regulatory applications, including variations, renewals, and responses to health authority questions. * Ensure regulatory dossiers remain compliant and up to date for EU, UK, and Switzerland markets. *...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description We're looking for a Clinical Research Associate II (CRA II) to join our growing Clinical Operations team in Italy. If you're passionate about clinical research, enjoy building strong site relationships, and want to contribute to studies that make a real difference for patients...