Regulatory Reporting Jobs in Sachsen

1 - 7 von 7

Suchergebnisse - Regulatory Reporting Jobs in Sachsen

Senior Softwareentwickler - Java / Spring / SQL / Linux (m/w/d)

apartmentWorkwiseplaceLeipziglanguagestudentjob.deevent_availableheute

Über das UnternehmenCURENTIS ist ein Produkt- und Consultingunternehmen für Regulatory Reporting, Sustainable Banking, Information Security und Anti-Financial Crime.Unsere Produktlösungen setzen Maßstäbe für digitale Prozesse, die die KYC...

Clinical Research Associate II (CRA II) / Klinischer Monitor – Full-Time or Part-Time Available (m/w

apartmentThermo Fisher ScientificplaceLeipzigevent_availablegestern

clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation.. Acts as a site processes specialist, ensuring that the trial is conducted in accordance...

Group Regulatory Affairs Specialist Class II (m/f/d)

apartmentOntex GroupplaceGroßpostwitzlanguagejob24.deevent_available2 Wochen alt

and report conclusions and recommendations. • Identifies the need for new regulatory procedures and SOPs and assures that departmental SOPs are developed to ensure regulatory compliance and participate in development and implementation. • Identifies...

Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d

apartmentThermo Fisher ScientificplaceDresdenevent_availablegestern

EHS Manager (m/w/d)

apartmentFahrzeugbau/-zulieferer KarriereplaceZwickauevent_available3 Tage alt

and partners with site leadership team to reduce operational risks. The Site EHS Manager acts as the motor for EHS at the site, ensuring implementation of corporate standards, regulatory requirements and best practises. The Site EHS Manager develops smart...

Principal Clinical Research Associate (PCRA) / Klinischer Monitor – Full-Time or Part-Time Available

apartmentThermo Fisher ScientificplaceDresdenevent_availablegestern

management for complex clinical trials. Acting as a subject-matter expert and site process specialist, you will ensure trials are conducted in accordance with the approved protocol, ICH-GCP, applicable regulatory requirements, and internal SOPs—ensuring...

Senior Clinical Research Associate (Sr CRA) / Senior Klinischer Monitor – Full-Time or Part-Time Ava

apartmentThermo Fisher ScientificplaceLeipzigevent_availablegestern

deliver high-quality, inspection-ready clinical trials. What You’ll Do Perform site monitoring activities (on-site and remote) using a risk-based monitoring approach Ensure protocol, ICH-GCP, regulatory, and SOP compliance at investigator sites...