Freelance Designer
Watson Creative
Job Level
Mid-LevelSenior
About the role
- Critically evaluate existing epidemiological evidence and generate new insights through study protocols, registry analyses and other relevant data sources
- Design epidemiological studies to improve disease understanding and support strategic evidence needs
- Identify and apply appropriate Real World Evidence (RWE) approaches to optimize study design and execution, including pragmatic and hybrid trials
- Lead the development and execution of Evidence Generation Plans aligned with product strategy
- Collaborate with academic partners, KOLs, registry holders and CROs to develop RWE research plans and manage outsourced studies, ensuring methodological rigor
- Interpret and communicate study findings across cross-functional teams and contribute to the dissemination and strategic use of RWE in regulatory, reimbursement and clinical decision-making contexts
Requirements
- Minimum 4-year experience in epidemiology, pharmacoepidemiology, non-interventional studies (prospective studies, patient registries, retrospective database studies)
- Experience in RWE generation in biopharmaceutical industry or CROs
- Knowledge of registry studies and phase 4 trials
- MSc in Health Science disciplines (Medicine, Veterinary, Biology, Biotechnology, Pharmacy)
- PhD in Epidemiology/Pharmacoepidemiology/Public Health/Outcomes Research is an advantage but not mandatory
- Strong communication skills
- Fluent in English
- Integrity, professionalism, and adherence to compliance standards
- Curious, proactive, and open to learning in a professional environment where quality and compliance matter
