Metronomia Clinical Research
Senior Statistician (UK based)
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Senior Statistician (UK based)
Location: UK Employment type: Full-time
We are looking for an enthusiastic and dynamic Statistician with demonstrable experience in biostatistical services to join our team.
About the Role
The Senior Statistician will play a key role in supporting our biotech and pharmaceutical clients by delivering high-quality statistics services across the entire clinical trial lifecycle.
Responsibilities
- Independently developing Statistical Analysis Plans (SAPs), including:
- Definition of estimands
- Statistical analysis models
- Hypothesis tests
- Creation of mock shells
- Coordinating project teams of statisticians and statistical programmers to ensure the quality and timeliness of deliverables, including:
- SDTM datasets
- ADaM datasets
- Treatment-As-Drawn (TFLs) documentation
- Performing quality control of datasets and TFLs, including:
- Independent reprogramming of complex ADaM datasets
- Statistical analyses in SAS
- Acting as the primary point of contact for clients on all statistics-related inquiries
- Supporting statistical consulting services, including:
- Study design advice
- Sample size calculations
- Protocol development (with focus on estimands)
- Chairing Data Review Meetings (DRMs), with responsibility for:
- Decision-making
- Corresponding documentation processes
- Authoring or reviewing the statistical sections of clinical trial reports (CTRs)
- Providing independent data monitoring committee (I/DMC) support, including:
- Creation of (I)DMC reports
- Hosting of (I)DMC meetings
- Managing project budgets, including:
- Preparation of performance reports
- Initiation of change orders when necessary
- Participating in bid defence meetings and presenting biostatistical services including:
- Statistical programming capabilities
- Representing Metronomia's biostatistics team in:
- Regulatory inspections
- Customer audits
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Requirements
- A university degree in statistics, mathematics, mathematical biometrics, or a comparable qualification
- At least three years' professional experience as a statistician, preferably in:
- A CRO (Contract Research Organisation)
- Pharmaceutical industry environment
- With previous project responsibility
- Strong knowledge of regulatory guidelines and CDISC (Clinical Data Interchange Standards Consortium) standards
- Excellent communication and interpersonal skills
- Enjoyment of collaborating closely with clients
Benefits
- Recognition and family-friendly culture: Hybrid working models with a supportive workplace that values individual contributions
- Competitive rewards: Remuneration and benefits package reflecting your contributions
- Wellbeing support: Comprehensive benefits package designed to support overall health
- Flat hierarchies: Collaborative team environment where everyone’s contributions are valued equally
- Engaging work: Thorough onboarding and opportunities for:
- Internal and external training
- Continual professional development
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About Metronomia
Since 1990, Metronomia has stood for quality, competence, continuity and customer-centric excellence in clinical research data management, statistical services, and medical writing. As a growth-oriented medium-sized company, we operate internationally with over 155 employees. Our successes are built on the commitment and expertise of our people.
A dedicated employer of choice, Metronomia values diversity and inclusiveness in recruitment. If you require any reasonable adjustments during the application or interviewing process, please notify us.
For further enquiries, contact our HR Managers:
- Lachaé Leo (lleo@metronomia.net)
- Christoph Hortian (chortian@metronomia.net)
Visit www.metronomia.net to explore our career opportunities.
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