1201 F. Hoffmann-La Roche AG
Statistician(m/w/x)
Full-timeOn-siteEntry Level
Basel
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F.F. Hoffmann-La Roche AG
Statistician(m/w/x)
Basel
Full-timeOn-siteExperienced
Nejo AI Summary
Clinical trial design and statistical analysis for life-changing medicines. MSc/PhD in Statistics and 2+ years in clinical trials required. SAS/R proficiency, familiarity with ICH/GCP.
Requirements
- MSc or PhD in Statistics, Biostatistics, or related quantitative field
- Minimum 2 years relevant experience in clinical trial statistics
- Familiarity with ICH guidelines, GCP, and regulatory requirements
- Strong understanding of statistical principles and methodology
- Proficiency in SAS and/or R
- Familiarity with CDISC standards
- Capacity for independent thinking and decision-making
- Excellent strategic agility, problem-solving, and critical thinking skills
- Respect for cultural differences in global workplace interactions
- Excellent verbal and written communication skills, presentation and writing
- Ability to explain complex technical concepts in clear language
- Experience working in cross-functional teams
- Effective communication skills, translating complex statistical concepts
- Experience with multiple phases of drug development
- Excellent communication skills, influencing and translating complex data
- Strategic mindset for portfolio-level decisions
Tasks
- Contribute to trial design using standard statistical methods
- Draft and review protocols, statistical analysis plans, and case report forms
- Perform or support statistical analyses as per statistical analysis plans
- Escalate issues when needed
- Represent Biostatistics and PDD at the Study Team level
- Ensure statistical and scientific rigor of study deliverables
- Collaborate with study team members to meet deliverables
- Summarize findings clearly with support from senior colleagues
- Contribute to CSR development and regulatory responses
- Address moderately complex statistical or data issues
- Seek guidance for novel or ambiguous situations
- Adhere to functional standards through peer review
- Participate in mentoring relationships to build expertise
Work Experience
- 2 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
- CDISC standards
- ICH guidelines
- GCP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of F. Hoffmann-La Roche AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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Statistician(m/w/x)
Basel
Full-timeOn-siteExperienced
Nejo AI Summary
Clinical trial design and statistical analysis for life-changing medicines. MSc/PhD in Statistics and 2+ years in clinical trials required. SAS/R proficiency, familiarity with ICH/GCP.
Requirements
- MSc or PhD in Statistics, Biostatistics, or related quantitative field
- Minimum 2 years relevant experience in clinical trial statistics
- Familiarity with ICH guidelines, GCP, and regulatory requirements
- Strong understanding of statistical principles and methodology
- Proficiency in SAS and/or R
- Familiarity with CDISC standards
- Capacity for independent thinking and decision-making
- Excellent strategic agility, problem-solving, and critical thinking skills
- Respect for cultural differences in global workplace interactions
- Excellent verbal and written communication skills, presentation and writing
- Ability to explain complex technical concepts in clear language
- Experience working in cross-functional teams
- Effective communication skills, translating complex statistical concepts
- Experience with multiple phases of drug development
- Excellent communication skills, influencing and translating complex data
- Strategic mindset for portfolio-level decisions
Tasks
- Contribute to trial design using standard statistical methods
- Draft and review protocols, statistical analysis plans, and case report forms
- Perform or support statistical analyses as per statistical analysis plans
- Escalate issues when needed
- Represent Biostatistics and PDD at the Study Team level
- Ensure statistical and scientific rigor of study deliverables
- Collaborate with study team members to meet deliverables
- Summarize findings clearly with support from senior colleagues
- Contribute to CSR development and regulatory responses
- Address moderately complex statistical or data issues
- Seek guidance for novel or ambiguous situations
- Adhere to functional standards through peer review
- Participate in mentoring relationships to build expertise
Work Experience
- 2 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
- CDISC standards
- ICH guidelines
- GCP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of F. Hoffmann-La Roche AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein führender Anbieter von pharmazeutischen Wirkstoffen und setzt sich für die Gesundheitsversorgung weltweit ein.
Not a perfect match?
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