Associate Director, Global Real-World Evidence (RWE) Science

CSL; Barcelona; Sur place; EUR 120 000 - 180 000; Plein temps

Résumé du poste

Seqirus seeks an Associate Director, Real World Evidence Science in Barcelona to lead global RWE programs for vaccine products within the Center of Outcomes Research and Epidemiology (CORE).

The role drives strategy, designs complex studies, and coordinates with Medical Affairs, Regulatory, Market Access, and external partners to generate impactful evidence informing practice and policy.

Qualifications

• MD/PhD or Master in Epidemiology, Biostatistics, Public Health, or related field.
• 8–10 years of epidemiology/outcomes research, 5+ years in pharma/biotech.
• Experience designing/prospective epidemiology studies and analyses with large databases.
• Expertise in Phase IV/outcomes research methods.
• Experience with real-world data sources (claims, EHR).
• Proficiency in SAS/SQL/R/Stata; strong publications.
• Cross-functional project leadership in global settings.
• Excellent communication and stakeholder management.
• Ability to translate science for diverse audiences.

Responsabilités

• Lead planning, design, execution, and oversight of RWE studies across vaccine programs.
• Drive global RWE strategy within CORE and Medical Affairs.
• Collaborate with Medical Affairs, Market Access, Regulatory, Clinical Development, and others.
• Oversee study feasibility, protocol development, reports, and evidence packages.
• Manage CROs and external partners for high-quality execution.
• Support health authority interactions and dissemination of results.

Connaissances

Epidemiology

Biostatistics

Public Health

RWE/Pharmaceutical Industry

SAS/SQL/R

Leadership

Communication

Formation

MD/PhD/Master in Epidemiology/Related Health Science

Outils

SAS

SQL

R

Stata

Description du poste

Seqirus seeks an Associate Director, Real World Evidence Science in Barcelona to lead global RWE programs for vaccine products within the Center of Outcomes Research and Epidemiology (CORE).

The role drives strategy, designs complex studies, and coordinates with Medical Affairs, Regulatory, Market Access, and external partners to generate impactful evidence informing practice and policy.