Strong experience in biostatistics for clinical and non-clinical studies
She has extensive expertise in phases I-IV of clinical trials, with a deep understanding of statistical coordination, data management, and programming
Background in SAS programming and statistical software like WinNonlin and ADDPLAN allows her to deliver precise statistical analyses and validate clinical study reports effectively
Holds a Ph.D. in Mathematics, providing her with a strong foundation in statistical methodologies
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Overview
- Availability
- Asap; full-time; onsite & remote
- Qualification
- Ph.D. in Mathematics
- Language Skills
- German (native), English (business fluent)
- Relevant Expertise
- Biostatistics, Clinical Studies, Statistical Analysis Plan, SAS Programming, SOP Writing, Statistical Consulting, Regulatory Knowledge, Clinical Study Reports, Project Management, Pharma
Key-Facts
Extract from Previous Activities
Universities
Statistician
Consultant to Ph.D. Students and Faculty (mostly medical but also social sciences)
Integrity of statistical results
CRO Company
Biostatistician
Early phase I and II studies
Protocol development
CRF development
SAP
Table shells
Biopharmaceutical Company
Biostatistician
Acute Myeloid Leukemia, Matching Case-Control Study
SAP and CRF development
Survival time to remission
University
Biostatistician
Testing the biomechanical properties of the implant in minipigs after 24 and 48 weeks. Length of the study is due to the large number of animals involved
Ongoing cooperation in the Scientific research of the department, consultation: Study design, Data management, Sample size, Statistical analysis, Quality control, Interpretation of results, Co-author publication
CRO Company
Biostatistician
Install Network Meta Analysis (NMA) procedure
Contents of template
Statistical procedures to be included
SAS code for analysis