Senior Data Scientist with focus Clinical Statistics (f/m/d - part/full-tim
at Staburo GmbH
81549 München, Bayern, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 18 Feb, 2025 | Not Specified | 18 Nov, 2024 | 3 year(s) or above | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
YOUR PROFILE
- Master´s degree in statistics, mathematics, or comparable studies or PhD
- At least three years of professional experience as a statistician with responsibility for clinical studies
- Very good methodological knowledge of basic and advanced statistical methods in the field of clinical trials
- Very good IT skills, especially with statistical analysis tools (SAS, R)
- Knowledge of relevant terminology in clinical and non-clinical research
- Knowledge of relevant guidelines GCP, ICH
- Quick comprehension and analytical thinking
- Team player with high degree of initiative
- Good English skills, German is an advantage
ABOUT US
Staburo GmbH is a data science company, specialized in statistical consulting, programming and bioinformatics for healthcare projects. Our core competencies include Clinical Statistics, Translational Medicine & Biomarkers, Phase I & Pharmacokinetics/-Dynamics, Data Transparency & Disclosure Services, Health Technology Assessment and Bioinformatics. Our customers are international pharmaceutical companies, CROs, biotech companies and medical device manufacturers. Our steadily growing team supports our clients efficiently from study design to data analysis and finally the disclosing and posting of trial results
Responsibilities:
- Analysis of project data (e.g. trial data) and data processing
- Statistical programming, development of reusable programs (e.g. functions, macros), data visualization, program validation, output generation
- Support non-clinical / clinical development in all phases, study planning (protocol, study design), sample size, reporting, analysis plan (e.g. SAP)
- Customer consulting and direct point of contact
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
81549 München, Germany