Frank Biedermann Email & Phone Number

Düsseldorf, Nrw, De

Kreisfreie Stadt Aachen Und Umgebung, Deutschland

- Collaborates with different teams/users to help them leverage data and advanced analytic solutions in their products/areas- Gathers requirements, build data models, design roadmaps and outlines architectural designs to help teams achieve their goals - Builds ETL jobs based on jointly defined requirements along the data pipeline - Works closely with both the backend developers as well as the IT group- Design and build CI/CD pipelines for data and application build process- Build Docker custom images and setup Kubernetes cluster - Supports the bug fixing and performance analysis along the data pipeline - Brings experience of modern database technologies (SQL and noSQL), Data Lake technologies and modern data management techniques to the development team - Builds stored procedures/functions packages, shell scripts/batch files as required- Reaches out to the best outsourcing providers, programming and analytics associations and academia partners- Technical- consultant and project manager for the Bio2Treat project (cooperation project between the Bundesministerium für Bildung und Forschung - BMBF, Uniklinikum RWTH Aachen und Grünenthal)

Kreisfreie Stadt Aachen Und Umgebung, Deutschland

- Design, develop, document, validate and maintain (SAS) computer programs to derive, store, analyse and report clinical data- Develop, apply and maintain standard SAS programs, functions and macros- Perform data pooling and data mapping- Manage clinical data exchange activities with CROs and external partners- Develop, apply and maintain Data Warehouse programs, jobs and workflows

Kreisfreie Stadt Aachen Und Umgebung, Deutschland

- Implementation, maintenance and operation of Data Science systems and tools- Work according to ICH-GCP guidelines as well as the internal quality system- Design, develop, maintain and/or validate programs to derive, store, map, analyze and report clinical data- Contribute to the definition, implementation and maintenance of data standards (CDASH, SDTM, ADaM)- Manage clinical data exchange activities

Kreisfreie Stadt Aachen Und Umgebung, Deutschland

- Implement e-Clinical solutions for clinical trials- Manage e-Clinical solutions within Data Management (Medidata, ePRO system, Clinical Data Warehouse and DS Navigator)- Manage operational aspects for eCRF, ePRO, CDASH, SDTM and other clinical data on trial level- Provide support for defining, implementing and maintain-ing data standards (e.g., CRF, CDASH, SDTM) - Provide strategic and operational input related to e-clinical solutions on project and study level

Aachen

- State-of-the-art SAS programming (programming of statistical analyses, tables, figures and listings)- Developing, applying and maintaining standard SAS programms and macros- Defining, implementing and maintaining data standards (SDTM, ADaM) and SAS dataset structures.

- Responsible for the introduction, maintenance, change, validation, and retirement of special soft-/hardware and computerized systems in Compound Development and Branding- Main contact person for SAS software at Grünenthal- Technical lead for: the SAS EBI environment in Compound Development and Branding, the patient profile viewer solution SAS JMP Clinical, the evaluation of SAS JMP Genomics- Technical consultant for the clinical data warehouse (SAS Drug Development): Defined and implement core data warehouse folder structures and permissions, Defined and implement metadata for clinical projects/trials and data standards, Created SAS modules for: setup a new trial, read in data standards, Created SAS macros for: export/import CPT/XPT and Microsoft office files, data comparison, Created processes for: setup the programming environment and Warning/Error handling

- Implementation and rollout of the SAS Business Intelligence Suite and SAS Data Integration Server- Direct support of business process improvement group in evaluating, maintaining and/or implementing: the statistical computing environment, SAS DI processes, SAS BI reports, dashboards and STPs, SAS custom web portlets, SAS JMP for the SixSigma project, Pharmacometrics software- Technical project lead for: safety reporting portal, clinical genomics projects, mid-term planning process- Member of the Grünenthal CDISC group- Technical consultant for the clinical data warehouse project (SAS Drug Development)

- Setting-up and programming of clinical trial outputs/analyses for phase I-III- Working and structuring data in accordance with CDISC conventions- Extensive experience in creation of databases for ISS and its subsequent analyses- Direct support for Clinical Operation's Groups in Evaluating Drug Accountability Data as per ICH E6- Created randomization macro and drug accountability process in SAS- Created SAS macro for standard tables, listing and figures of clinical study reports in accordance with ICH E3- Set-up of validation process in accordance with 21 Part 11 for SAS standard programs/macros- Derivation of datasets in preparation for PK/PD and Population-Pharmacokinetics Modelling and Simulation Analyses- Implementation of an new statistical computing environment for biometrics- Rollout from SAS Foundation and Enterprise Guide on 50 clients an one server Setup a new data repository Migrating SAS data, programs and macros from Unix to Windows