Data Scientist with focus Pharmacokinetics (f/m/d - part/full-time)
at Staburo GmbH
81549 München, Bayern, Germany -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 01 Aug, 2024 | Not Specified | 05 May, 2024 | N/A | 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
- University degree in data science, pharmacology, mathematics, computer science, or equivalent education with a good knowledge in statistics
- Knowledge of PK principles and popPK analysis
- Experience with Phoenix WinNonlin, NONMEM is an advantage
- At least two years of experience in SAS programming and clinical research
- Excellent working knowledge of clinical trial documents (CSP, SAP, CTR)
- Very good knowledge of clinical data
- General understanding of global regulatory guidance on pharmacometrics analyses and reporting
- Knowledge of CDISC standards is a plus
- Experience in R programming is an advantage
- Strong analytical and quick-learning skills
- Precise and accurate way of working
- Team player and a high degree of initiative
- Good English skills, German is a plus
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:
- Conduct data analyses including non-compartmental analyses, modelling & simulation
- Statistical programming with SAS or R, development of reusable programs (e.g. macros), data processing, data visualization, and output generation
- Specification and creation of analysis datasets
- Validation of datasets and outputs
- Support non-clinical / clinical development in all phases
- Develop PK part of trial protocols and statistical analysis plans
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
81549 München, Germany