Coronado Research is a consultancy-led, AI-enabled CRO that supports pharmaceutical, biotech, and med-tech companies in accelerating evidence generation through advanced data science, regulatory expertise, and real-world evidence (RWE) strategy. Our teams combine clinical, regulatory, and analytical excellence to help sponsors meet the evolving demands of modern drug development. 

We're expanding our epidemiology function to support projects around Safety, RWE and Regulatory. These roles are ideal for Safety Epidemiologists who want to work at the intersection of regulatory science, real-world data, and trial design innovation. 

You'll collaborate with global sponsors and internal AI-driven data teams to operationalize diversity and enrolment goals using real-world data (RWD), applying target trial emulation principles to bridge clinical trial and real-world populations. 

Key Responsibilities 

• Define the Intended Use Population (IUP): Interpret clinical trial protocols and translate eligibility criteria into real-world definitions using RWD sources. 

• Develop Epidemiology Strategy Plans (ESP): 

• Conduct targeted literature reviews and synthesise background including  epidemiologic and demographic data. 

• Design RWD analyses  

• Draft and QC the Epi Strategy Plan document. 

• Lead Data Interpretation & Reporting: 

• Develop and QC analysis plans for enrollment goal modeling. 

• Review RWD outputs and interpret data  

• Write and QC the final Epidemiology Report, summarising findings and enrollment goals. 

• Collaborate Cross-Functionally: Work with biostatisticians, data scientists, regulatory, and clinical teams to ensure evidence strategies align with Regulatory guidance and sponsor objectives. 

   

About You 

• Postgraduate qualification (MSc or PhD) in Epidemiology, Biostatistics, or related field. 

• Experience in real-world data analytics (e.g., EHR, claims, registries, or linked datasets). 

• Understanding of target trial emulation and causal inference methods. 

• Familiarity with FDA/EMA regulatory frameworks, particularly regarding diversity, inclusion, and safety monitoring. 

• Strong scientific writing, interpretation, and QC skills. 

• Collaborative, detail-driven, and comfortable working across global, multi-functional teams. 

   

Engagement Model 

• Flexible engagement: Full-time, part-time or Consultant  

   

Why Join Coronado 

At Coronado Research, you'll join a global network of clinical data experts, regulatory strategists, and AI innovators redefining how evidence is generated. You'll contribute to meaningful projects that help improve diversity, inclusion, and safety in clinical trials - shaping the next generation of real-world-driven research.