I contribute to clinical research with expertise and empathy. And I do it
RWE Specialist
Primary Location: United Kingdom, Remote Additional Locations: United Kingdom, Sheffield; United Kingdom, Harrow; United Kingdom, Littlehampton(Closed); United Kingdom, London; United Kingdom, Navigation House; United Kingdom, Uxbridge; United Kingdom, Worthing Job ID R0000036434 Category Regulatory Affairs Date Posted 11/03/2025Overview
As part of Parexel Consulting, you will play a vital role in helping biopharmaceutical and medical device companies navigate the complex and ever-changing regulatory landscape. Drawing on your scientific, technical, and regulatory expertise, you will work closely with clients to develop and implement regulatory strategies that bring their products to market faster and keep them there.
We value collaboration, innovation, and continuous learning. As a member of our team, you will partner with a diverse group of clients, and be exposed to various product types and therapeutic areas. You will also develop your skills through challenging assignments and mentorship from experienced regulatory professionals. Plus, you will enjoy the flexibility of working remotely while still being part of a supportive and dynamic team.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
- Communicator
- Detail-oriented
- Problem-solver
- Relationship-builder
- Results-driven
- Strategic
About This Role
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
- Understand and be familiar with the licensed RWD database(s) relevant to the organization’s clinical research initiatives
- Independently identify, access, and assess in-house real-world data sources (EHRs, claims, registries, etc.) relevant to clinical trial populations and endpoints
- 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
- Critically evaluate data quality, completeness, and suitability for specific trial design questions
- Develop RWD exploration plans
- Clean, process, and harmonize raw RWD for analysis, applying data governance and privacy standards
- 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
- Prepare clear, concise evidence summaries and visual reports to inform protocol development (inclusion/exclusion criteria, endpoints, comparator selection, feasibility assessments, etc.)
- Collaborate cross-functionally with clinical, regulatory, biostatistics, and medical teams to ensure alignment with study goals and timelines
- Stay current on RWD methodologies, regulatory guidance, and technological advances in the field
- Ensure all work supports timely, high-quality decision making for new clinical trial design and execution
- Develop innovative RWD analytical tools to support evolving clinical trial needs
- Conduct independent assessments of data sources to determine relevance, quality, and utility for real-world evidence generation
- Incorporate input from internal subject matter experts (SMEs) to ensure alignment with RWE/RWD best practices and strategic objectives
Qualifications
- Advanced degree in Epidemiology, Biostatistics, Public Health, or related field preferred
- 3–5 years of relevant experience in real-world data analytics or related field
- Proficiency in SAS, R, Python, and SQL
- Experience working with healthcare data sources including EHRs, claims, and registries
- Strong understanding of clinical trial design and real-world evidence methodologies
- Demonstrated ability to develop and apply innovative analytical tools and approaches
- Excellent communication and collaboration skills
- 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.
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