We are seeking a highly qualified and experienced pharmacoepidemiology or public health professional to deliver a comprehensive Real‐World Evidence (RWE) in Pharmacoepidemiology course in Spain. The adecuado candidate will possess deep expertise in real‐world data (RWD) sources, study design, and advanced analytical methods, with a proven ability to translate complex statistical and regulatory concepts into practical, actionable training for healthcare and research professionals.

Key Responsibilities

- Design and deliver an in‐depth training program on RWE, covering foundations of RWD, study designs (cohort, case‐control, cross‐sectional), data quality and governance, and bias/confounding control.
- Develop and utilize a range of training materials, including detailed presentations, hands‐on data analysis labs (R/Stata/SAS/Python), real‐world case studies, and practical exercises on protocol development and analysis plans.
- Facilitate interactive sessions to help participants evaluate drug safety and effectiveness, interpret results, and translate evidence into regulatory, clinical, and public‐health decisions.
- Guide participants through advanced methods such as propensity score techniques, instrumental variable analysis, sensitivity analyses, and transparent reporting frameworks.
- Provide expert insight into EU/Spain‐relevant topics: GDPR for health data, EMA guidance, HTA considerations, pharmacovigilance signal evaluation,



and emerging applications of RWE.
- Conduct assessments and lead discussions to measure trainees' understanding of study design, data handling, and result interpretation, culminating in project presentations.
- Collaborate with the client to align the training with participant backgrounds (epidemiology, clinical, regulatory, analytics) and with accreditation expectations (CPD/BAC/ISO standards).

Requirements

- 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.

📌 Trainers/Instructors For Real‐world Evidence In Pharmacoepidemiology (Andalucía)
🏢 Peoplique | HR Solutions
📍 Andalucía