Jobs 871 bis 880 von 1.167 (dupliziert 1.038)
PharmiWeb - May
monitoring and adherence Ensure the statistical programming systems, processes and deliverables are aligned with the relevant regulatory requirements, for instance: Clinical study reporting, e.g. ICH E3 Electronic recordsVor 60+ Tage
Principal Statistical Programmer
PharmiWeb - May
aligned with the relevant regulatory requirements, for instance: Clinical study reporting, e.g. ICH E3 Electronic records handling, e.g. Chapter 21 of the US Code of Federal Regulation - Part 11 Electronic submissionVor 60+ Tage
Senior Scientist Analytical Development of Biologicals
AbbVie - Ludwigshafen am Rhein
pharmaceutical industry with exposure to analytical development across all stages of development, including regulatory filings Sound expertise in development of complex analytical methods and practical experience with test methodVor 60+ Tage - Preview
All rights reserved - Bayreuth
expected to ensure that the contractual and regulatory HSE requirements are carried out at Project Level; Support preparation of the HSE Plans and other associated documents in compliance with PPL HSE Management System and HSEVor 60+ Tage
Werkstudent (w/m/d) Regulatory Affairs
Umantis - Hamburg
Hamburg Referenznummer: 80020972 Website: Ihre Aufgaben Unterstützung der Regulatory Affairs Manager im täglichen Tagesgeschäft Unterstützung bei der Dokumentenerstellung für ZulassungsaktivitätenVor 60+ Tage - Preview
Christoph Miethke Gmbh & Co.kg via Jobtome - Potsdam
Koordination von Produktbeschreibungen zwischen den Abteilungen Produktmanagement, Marketing und Regulatory Affairs in einem Redaktionssystem; Archivierung abgeschlossener Dokumentation; ProzessablaufbeschreibungVor 60+ Tage
Intercontinental Exchange - Frankfurt am Main
Responsibilities Identify and develop relationships with influencing groups within the relevant market - industry groups and regulatory bodies Work with marketing and communications teams to identify optimal ways to develop ICE brandVor 60+ Tage
PharmiWeb - May
specifications, and perform statistical analyses. Review and contribute to study reports and clinical and statistical sections of regulatory submission dossiers, lead electronic submissions of clinical data to regulatory authoritiesVor 60+ Tage
Associate Director In Vitro DMPK
PharmiWeb - Beelitz
discovery and development. Contributing to study reports and regulatory documentation such as SOPs and INDs. Leading a lab of 3 technicians. Ensuring studies comply with German law and regulations. QualificationsVor 60+ Tage
Hobson Prior - Frankfurt am Main
90000.00 - €100000.00 per annum Permanent Frankfurt am Main, Hessen Regulatory Affairs, Labelling Posted: 02/09/2020 BBBH14951 Hi I'm , I manage this role This vacancy has now expired. Please seeVor 60+ Tage