Clinical trial:
Conception of study protocol, statistical evaluation plan, SAS programming incl. Mock-up TLF, data review meeting, SAS analysis, evaluation and interpretation of the results from a biometric point of view, statistical report, participation in clinical report
Diagnostic study:
Concept, evaluation plan, analysis
Diagnostic study:
New analysis of already evaluated data: Examination of the quality of the data, determination of influencing factors (center, measurement day, ...) that could have led to distortions. New analysis after correction
Diagnostic study:
Method development, joint scientific publications
Diagnostic study:
Analysis of given data, report, conclusions regarding future studies
Clinical trial, Pharmaceutical industry:
Subcontractor for CRO, taking over all statistical services
Clinical trail: Pharmaceutical industry:
independent statistician in the DSMB
Medical device study:
Sponsor contractor, takeover of all statistical services
Research laboratory:
Evaluation of data analysis procedures. Determination of sources of error
Clinical research: Establishment of statistical analysis methods for the evaluation of mutagenicity experiments, implementation of training
Clinical research:
Transfer of the biometric part (biometric part of the study plan, statistical evaluation plan, pharmacokinetic analyzes, proof of bioequivalence, report)
Statistics training:
Introduction to statistical methods and 2 statistical programs (2-day course for scientific managers of a company)
Work contract with the university: statistical support for third-party funded projects by university research groups
Expert activity:
Preparation of expert opinions on publications (e.g. marketing documents) from a statistical / biometric point of view