Benjamin Pohl

same work as detailed below with Chiltern. Only the company name has changed.

As a CDA-2 I actively work together with the Project Data Manager as his/her substitute on study setups, and am responsible for generation and maintenance of the eCRF Design Specifications, Edit Check Specifications and coordination of the User Acceptance Testing to meet project timelines. Further tasks encompass: Data cleaning and validation, report generation, quality control of documents, filing in the trial-master-file and data reconciliations (SAE- & external vendor data).

As a CDA-1 I was responsible for laboratory management (data entry, QC and tracking of lab normal ranges), filing of documents, discrepancy management in the EDC (raising and resolving data management queries) and trainee for data management documents (DMP, UAT Plan, Edit Check Specifications, eCRF Specifications).

Data cleaning and preparation for statistical analysis, programming in company-specific SAS-environment, SAS-programming of tables and listing together with macros for report generation, basic validation of statistical results, quality control of the numbers for admission-relevant documents, consolidation of protocol deviations and data management queries in an active study, checked Trial-Master-File (TMF) and CRF for completeness, acquisition and distribution of literature requested by colleagues.

Preparation and import of Excel-data into SAS 9.2, programming of descriptive analyses with the support of SAS macros, programming of inferential statistical analyses by use of simple SAS procedures (PROC TTEST, PROC NPAR1WAY...), Progamming of simple SAS macros, Export analyses results through SAS/ODS.

Contents of teaching: Theoretical medicine, Pathology, Documentation, Mathematics, Descriptive Statistics, Epidemiology, Informatics, Healtcare organisation and laws, SAS programming, Software programming (Visual Basic, Phyton)