# Senior RWE Biostatistician

**Company**: Fortrea
**Location**: Maidenhead
**Experience**: senior
**Job type**: full-time
**Category**: Consulting
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Maidenhead/Senior-RWE-Biostatistician_265295?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_356e0a04-f11

## Description

As an experienced Senior RWE Biostatistician within our Consulting business, you will play a pivotal role in delivering complex Real-World Evidence (RWE), non-interventional, and low-interventional research studies for leading global pharmaceutical and biotechnology companies.

Working as a trusted client-facing consultant, you will help design innovative evidence-generation strategies, lead statistical analyses, and provide scientific expertise that supports regulatory, payer, and health technology assessment (HTA) decision-making.

In this role, you will apply advanced biostatistical methodologies to real-world data sources including claims databases, electronic health records (EHR), registries, and linked data assets.

You will contribute to the design, execution, and interpretation of high-impact studies while supporting business development activities, scientific publications, and internal innovation initiatives.

Your expertise will directly contribute to generating evidence that shapes healthcare decisions and improves patient outcomes worldwide.

**What else can you expect from us?**

- Rewarding and meaningful work in an established, diverse, highly profitable and respected global company

- Highly competitive compensation packages, including various local benefits such as pension contributions, complimentary health insurance plans, remote working allowances, and more

- A genuine work-life balance

- Flexibility in working hours

- A thorough onboarding program with support from your personal mentor

- A permanent employment contract with Fortrea

- Excellent training and career development opportunities, as well as support for continuing education

- Strong support from your Fortrea Line Manager, your team, and thousands of colleagues worldwide

**Your responsibilities**

- Lead the design, analysis, and interpretation of non-interventional and RWE studies utilizing claims, EHR, registry, and other real-world data sources

- Apply advanced causal inference and confounding-control methodologies including propensity score matching and weighting, inverse probability weighting, instrumental variable methods, marginal structural models, and difference-in-differences approaches

- Design and support innovative evidence-generation strategies, including target trial emulation, external control arms, and synthetic control methodologies

- Develop and review Statistical Analysis Plans (SAPs), statistical sections of protocols, estimands, and study design documentation

- Ensure alignment of study methodologies and outputs with applicable regulatory guidance and RWE frameworks, including FDA and EMA expectations

- Perform statistical quality control and promote analytic reproducibility and transparency across client engagements

- Deliver strategic, scientific, and methodological expertise to clients and project teams

- Manage project teams responsible for statistical deliverables while providing guidance, oversight, and mentorship

- Support proposal development, budgeting, bid defenses, capability presentations, and other business development activities

- Contribute to internal innovation initiatives, methodological best practices, scientific publications, and conference presentations

- Mentor and develop junior statisticians and analysts through coaching, training, and performance feedback

- Act as a subject matter expert for RWE methodologies and statistical best practices across the organization

**Your profile**

- Advanced degree in a relevant discipline such as Biostatistics, Statistics, Epidemiology, Health Economics, Data Science, Economics, Pharmacy, or a related field (Doctoral degree preferred)

- Minimum of 6 years of biostatistics experience with a Master's degree, including non-interventional/RWE research experience, or at least 4 years with a doctoral degree

- Proven experience leading statistical activities and delivering client-facing projects within a CRO, pharmaceutical, biotechnology, healthcare, or consulting environment

- Demonstrated expertise in applying biostatistical methods to RWE, epidemiology, and HEOR studies

- Experience utilizing real-world data sources such as claims databases, EHRs, registries, and OMOP or similar data models

- Strong understanding of causal inference, comparative effectiveness research, and bias-adjustment methodologies

- Experience developing SAPs, contributing to protocol design, statistical analysis, and reporting

- Programming proficiency in SAS and R (Python experience is considered an advantage)

- Knowledge of regulatory expectations and industry standards for RWE generation and evidence submissions

- Experience managing statisticians, analysts, or project teams and mentoring less experienced team members

- Strong client engagement, communication, presentation, and stakeholder management skills

- Excellent problem-solving ability, scientific curiosity, and attention to detail

- Business fluency in English, both verbal and written

## Skills

### Required
- Biostatistics
- Statistics
- Epidemiology
- Health Economics
- Data Science
- SAS
- R
- Python

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