Trainers/Instructors for Real‐World Evidence in Pharmacoepidemiology (Spain)
On-siteMarbella, Andalusia, Spain
Job Summary
Design and deliver a comprehensive Real-World Evidence course in Spain, covering study designs, data governance, and advanced analytics including propensity scores and instrumental variables. Develop training materials featuring hands-on labs in R/Stata/SAS/Python, case studies, and practical exercises on protocol development. Facilitate interactive sessions to evaluate drug safety, interpret results, and translate evidence into regulatory and clinical decisions. Provide expert insight on EU/Spain topics such as GDPR, EMA guidance, and pharmacovigilance signal evaluation. Conduct assessments and lead discussions to measure understanding, culminating in project presentations. Collaborate with the client to align content with participant backgrounds and accreditation standards.
Required Qualifications
- Proven experience as a trainer, instructor, or facilitator in pharmacoepidemiology, epidemiology, biostatistics, pharmacovigilance, or closely related RWE functions
- Substantial professional background in industry, CRO, academia, health systems, or regulatory/HTA bodies involving design and analysis of real‐world studies
- In‐depth knowledge of study design and advanced analytics for RWD, including propensity scores, instrumental variables, confounding/bias mitigation, and appropriate statistical testing
- Strong understanding of RWD sources (EHRs, registries, claims), data quality/integrity practices, and ethical/legal frameworks (GDPR; familiarity with EMA/HTA expectations)
- Excellent communication, presentation, and interpersonal skills, with the ability to engage a diverse audience of clinicians, researchers, analysts, and decision‐makers
- Ability to create engaging, interactive training using case studies, hands‐on exercises, and clear methodological explanations
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