When our values align, there's no limit to what we can achieve.
At Parexel, we believe in the power of real-world data to transform clinical research and improve patient outcomes. We are seeking a passionate and experienced RWE Specialist join our team and support the design and execution of clinical trials through advanced analytics and evidence generation. This role is ideal for someone who thrives in a collaborative, cross-functional environment and is driven by innovation and scientific rigor.
Title: RWE Specialist
Location: Remote – UK
Key Responsibilities
1. Understand and be familiar with the licensed RWD database(s) relevant to the organization’s clinical research initiatives
2. Independently identify, access, and assess in-house real-world data sources (EHRs, claims, registries, etc.) relevant to clinical trial populations and endpoints
3. Access and summarize non-patient-level real-world data (publications, aggregate claims or EHR analytics, federated learnings, external collaborations, etc.) relevant to clinical trial populations and endpoints
4. Critically evaluate data quality, completeness, and suitability for specific trial design questions
5. Develop RWD exploration plans
6. Clean, process, and harmonize raw RWD for analysis, applying data governance and privacy standards
7. Use SAS, R, Python and/or other advanced analytical programming tools to perform statistical analyses and generate insights on patient characteristics, treatment patterns, outcomes, and epidemiology
8. Prepare clear, concise evidence summaries and visual reports to inform protocol development (inclusion/exclusion criteria, endpoints, comparator selection, feasibility assessments, etc.)
9. Collaborate cross-functionally with clinical, regulatory, biostatistics, and medical teams to ensure alignment with study goals and timelines
10. Stay current on RWD methodologies, regulatory guidance, and technological advances in the field
11. Ensure all work supports timely, high-quality decision making for new clinical trial design and execution
12. Develop innovative RWD analytical tools to support evolving clinical trial needs
13. Conduct independent assessments of data sources to determine relevance, quality, and utility for real-world evidence generation
14. Incorporate input from internal subject matter experts (SMEs) to ensure alignment with RWE/RWD best practices and strategic objectives
Qualifications
15. Advanced degree in Epidemiology, Biostatistics, Public Health, or related field preferred
16. 3–5 years of relevant experience in real-world data analytics or related field
17. Proficiency in SAS, R, Python, and SQL
18. Experience working with healthcare data sources including EHRs, claims, and registries
19. Strong understanding of clinical trial design and real-world evidence methodologies
20. Demonstrated ability to develop and apply innovative analytical tools and approaches
21. Excellent communication and collaboration skills
22. Ability to work independently and cross-functionally in a fast-paced, matrixed environment
Why Parexel?
At Parexel, we put patients first. Our global team is united by a shared commitment to scientific excellence, operational integrity, and continuous learning. We foster a culture of inclusion, flexibility, and purpose-driven work—where your contributions directly impact the future of healthcare.