von Mandantenbuchhaltungen und monatlichen Reports Vorbereitung und Erstellung von Jahresabschlüssen (nach HGB und ggf. nach IFRS) sowie betrieblichen Steuererklärungen Erstellung von Umsatzsteuervoranmeldungen Durchführung
ensure that target enrollment will be met across the allocated countries.Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to
risk assessment requirementsPrepare and assist in the preparation of monthly reports, provide inputs for the finalization the yearlyEnd to end finance admin of PO’s, invoices, and trackersSupplier
environment by learning and adopting best practices. Follow and adhere to safety and security policies and procedures. Report immediately any safety or security issues or concerns. Your profile: Degree
environment by learning and adopting best practices. Follow and adhere to safety and security policies and procedures. Report immediately any safety or security issues or concerns. Your profile: Degree
Zugriff auf Gympass - das kostengünstige Wellbeing-Netzwerk mit Online- und Offline-Angeboten Ihre Aufgaben Telefonzentrale Betreuung von Besuchern und Handwerkern Recherche für die Reporter und Pflege
Conference on Harmonization (ICH) guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study
regulatory submissions, recruitment, case report form (CRF) completion, and data query resolutionCollaborating with experts at study sites and with client representativesDepending on client model there might
statistical reports. Requirements: BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form
Conference on Harmonization (ICH) guidelines.Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution.Collaborating with experts at study
in business development activities for target clients and contribute to advancing JLL's market position in sustainability.Regularly report on progress to the Head of Sustainability - EMEA Markets Advisory and
IQVIA is looking to appoint statistical programmers to utilize the SAS programming language to develop clinical study report materials according to the objectives of a clinical trial for regulatory
plus.Minimum 5 years’ experience managing complex ER cases including investigations, ill-health, dismissals, appeals, and report writing.Experience of a fast-paced matrixed organization is helpful.Training