08.06.24 | Vollzeit | Frankfurt am Main | PA Consulting Services GmbHStatements using IRIS Accounts Production, ensuring compliance with FRS 102 guidelines. - Adjustments and Reconciliations Prepare an extended trial balance for each set of financial statements to reconcile between the financial statements and GL data. - Disclosure Notes Draft disclosure notes related
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SESolid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid understanding of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SESolid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid understanding of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SESolid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid understanding of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SESolid understanding of FDA, EMA, ICH, and global regulations and guidelines Solid understanding of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Solid understanding of the drug development process from early- to late-stage development
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
Später ansehen06.06.24 | Vollzeit | Kaiserslautern | BioNTech SEGRAPH, SQL Solid understanding of FDA, EMA, ICH and global regulations and industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards Expertise in the requirements and technology required to support electronic submissions Experience in leading
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