Senior Health Outcomes & Real-World Evidence Manager

CSL; Kirkland; Presencial; CAD 90.000 - 130.000; Jornada completa

Descripción de la vacante

CSL is seeking a scientifically driven professional to lead Phase IV real-world evidence research focused on influenza vaccines. You will manage studies from concept to dissemination, coordinate with vendors and researchers, and ensure methodological rigor and regulatory compliance.

The role requires advancing evidence-generation plans, drafting study reports, and contributing to internal decision-making in a global, matrixed environment.

Formación

• Master's or PhD in public health, epidemiology, biostatistics, pharmacoepidemiology, health outcomes research, or a related field.
• Minimum of three years of observational research or real-world evidence experience.
• Strong understanding of Phase IV outcomes research and epidemiologic methods.
• Experience with claims data, EHRs, registries, or published literature.
• Proficiency in SAS/SQL/R/Stata; R preferred.
• Excellent written and oral communication for reports and publications.

Responsabilidades

• Manage Phase IV real-world evidence studies across the influenza vaccine portfolio.
• Serve as project manager and provide methodological recommendations for studies.
• Develop study concepts, protocols, and analysis plans; review reports.
• Manage vendors and collaborators; mitigate risks to timelines and budgets.
• Conduct literature reviews and meta-analyses to identify evidence gaps.
• Coordinate dissemination via abstracts, congress presentations, and manuscripts.
• Ensure compliance with epidemiologic reporting standards and regulations.

Conocimientos

Project management

Clear communication

Data interpretation

Analytical thinking

Educación

Master's or PhD in public health/epidemiology/biostatistics

Herramientas

SAS

SQL

R

Stata

Descripción del empleo

CSL is seeking a scientifically driven professional to lead Phase IV real-world evidence research focused on influenza vaccines. You will manage studies from concept to dissemination, coordinate with vendors and researchers, and ensure methodological rigor and regulatory compliance.

The role requires advancing evidence-generation plans, drafting study reports, and contributing to internal decision-making in a global, matrixed environment.