Description

After studying statistics in the UK, I worked 10 years as SAS programmer in clinical research. During that time I was assigned to multiple projects involving programming and/or projet management skills (supporting the CDISC standard team, writing URS/UAT for external systems, providing dahsboards for managers) and to studies activities (mapping, data quality control, TFL).

In the last few years, I mainly focused in developing training solutions to help SAS users in their data engineering and reporting activities.

I'm up for new data challenges.

Languages

French
Native or bilingual
English
Native or bilingual
German
Fluent

Workplace preferences

Can work on-site

Köln (up to 50km), Bruxelles (up to 50km), Munich (up to 50km), Luxembourg (up to 50km)

xxformat GmbH
Director
PHARMACEUTICALS INDUSTRY
January 2017 - Today (9 years and 4 months)
Cologne, Germany
Developing training solutions for SAS users to assist them in their data engineering and reporting activities.

Specifying, writing and documenting SAS programs to generate data quality control reports, to generate mapping specifications, and so forth.
SAS Programming SAS Training Data science
Bayer Vital GmbH
SAS Programmer
PHARMACEUTICALS INDUSTRY
January 2011 - June 2016 (5 years and 6 months)
Leverkusen, Germany
2014 to 2016 - SDTM Mapping for Phase I studies

From 2009 (while consultant for Datafocus GmbH) to 2014 - Supporting the standard team in the implementation of CDISC SDTM IG 3.1.2, 3.1.3 and 3.2 i.e. developing the process to provide standard metadata and control terms as SAS files.

Supporting colleagues in the implementation of study specific macros (study days computation).

Developing template and associated tools to specify trial design domains, check the data and create the final datasets.

Developing a tool to generate study metadata based on standard metadata.

Adapting and validating a standard program to extract Rave study metadata.

Providing input in standard maintenance systems and in programming environment systems (User Requirement Specification/URS, User Acceptance Test/UAT); Running test cases for internal system.

Supervising studies (programming perspective) outsourced in India, UK...

SAS Programming CDISC SAS
Datafocus GmbH
SAS Consultant
PHARMACEUTICALS INDUSTRY
June 2006 - December 2010 (4 years and 7 months)
Leverkusen, Germany
Working as SAS Consultant for Bayer Vital GmbH, starting from August 2006.

Statistical Programming: TFL

Validating SAS programs

Programming standard edit checks

Programming reports for managers

Supporting the standard team in the implementation of CDISC SDTM i.e. developing the process to provide standard metadata and control terms as SAS files.

SAS Programming CDISC Statistics SAS