TrainersInstructors for RealWorld Evidence in Pharmacoepidemiology (Spain)

We are seeking a highly qualified and experienced pharmacoepidemiology or public health professional to deliver a comprehensive RealWorld Evidence (RWE) in Pharmacoepidemiology course in Spain. The ideal candidate will possess deep expertise in realworld 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 indepth training program on RWE covering foundations of RWD study designs (cohort casecontrol crosssectional) data quality and governance and bias/confounding control.
  
• Develop and utilize a range of training materials including detailed presentations handson data analysis labs (R/Stata/SAS/Python) realworld 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 publichealth 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/Spainrelevant 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 expectaons (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 realworld studies.
  
• Indepth 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 decisionmakers.
  
• Ability to create engaging interactive training using case studies handson exercises and clear methodological explanations.