Sr/Principal Statistician (Sponsor-dedicated) Many possible locations (EMEA) - Early Phase
GBR-Remote, United Kingdom
R
GBP 53K-91K (estimate) Senior-level Full Time
Tasks
- Attend regulatory agency meetings
- Coach and mentor biostatistics staff
- Conduct verification and quality control of deliverables
- Coordinate biostatistics and statistical programming activities
- Create or review programming specifications
- Develop mock up displays for tables listings and figures
- Ensure outputs match SAP and specifications
- Follow SOPs and regulatory guidelines
- Generate randomization schedules
- Input to clinical study reports
- Lead integrated analysis projects
- Maintain project documentation and QC documents
- Manage scheduling across multiple projects
- Monitor study progress against milestones
- Participate in data monitoring committee activities
- Participate in data safety monitoring board
- Perform independent review of statistical work
- Prepare statistical analysis plans
- Provide statistical programming support
- Review SAS annotated case report forms
- Review database design and study documentation
- Serve as biostatistics representative on project teams
- Support business development proposals and budgets
- Support statistical tasks across project lifecycle
Perks/Benefits
- N/A
Skills/Tech-stack
Analysis Plan | Biostatistics | Clinical study | Clinical study report | Clinical trials | Data Monitoring | Data Monitoring Committee | Data Safety | Data Safety Monitoring Board | Data safety monitoring | ICH | Integrated Analysis | Quality Assurance | Quality Control | Randomization | SAS | SAS programming | Statistical Analysis | Statistical Analysis Plan | Statistical programming
Education
Related jobs
-
Analysis Plans | Biostatistics | CSR | Clinical trials | Data MonitoringCareer development | Inclusive culture | Peer recognition | Supportive line management | Technical trainingSenior-level Full TimeGBR-Remote, United Kingdom R1d ago
-
Principal Biostatistician - Remote (UK) GBP 57K-90K21 CFR | 21 CFR Part 11 | ADaM | Biostatistics | Blinded dataGreat Place to Work certification | Industry visibility | Remote work | Supportive teamSenior-level Full TimeLondon, England R1d ago
-
Principal Statistician - UK/Europe (Remote) GBP 49K-90KADaM | Analysis Plans | CDISC | Clinical Trial Design | Clinical trialRemote workSenior-level Full TimeVirtual United Kingdom R9d ago
-
Analysis Plan | Below Quantification Limit Data | Clinical studies | Compartmental Analysis | Dose ProportionalityContract based time and materials | Remote work flexibilitySenior-level Contract Full TimeUnited Kingdom - Remote R19d ago
-
Principal Bioinformatics Scientist GBP 83K-103KAWS | Agentic AI | Azure DevOps | Bioinformatics | Bulk transcriptomicsHybrid work modelSenior-level Full TimeSlough, Berkshire, United Kingdom R20d ago
-
Analysis Plan | Biostatistics | Clinical study | Clinical study report | Clinical trialsFully remoteSenior-level Full TimeGBR-Remote, United Kingdom R20d ago
-
Principal Statistical Programmer FSP GBP 53K-91KADaM | Ad Hoc Reporting | Ad-Hoc | CDISC | Clinical Study DataFully remote | Training development and supportSenior-level Full TimeUnited Kingdom R20d ago
-
Analysis Plan | Clinical study | Clinical study report | Clinical trials | Data MonitoringFully home basedSenior-level Full TimeGBR-Remote, United Kingdom R22d ago
-
ADaM | Clinical Trial Design | Clinical trial | Data Quality | Data VisualizationSenior-level Full TimeGBR-Remote, United Kingdom R26d ago
-
ADaM | Analysis Plan | CDISC | CRF | Data QualitySenior-level Full TimeGBR-Remote, United Kingdom R1mo ago
-
Analysis Plan | CUDA | Clinical Data Analysis | Clinical data | Clinical trialSenior-level Full TimeGBR-Remote, United Kingdom R1mo ago
-
Analysis Plan | Case Report Form | Data Monitoring | Data Monitoring Committee | Data SafetyCareer development | Inclusive culture | Peer recognition | Technical and therapeutic trainingSenior-level Full TimeGBR-Remote, United Kingdom R1mo ago