FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Real-World Evidence and pharmacoepidemiology, with a strong focus on designing and executing observational studies. Proficient in project management and collaboration with external partners while ensuring adherence to regulatory requirements and methodological standards.
Highest-signal resume keywords
Real-World Evidence ExpertisePharmacoepidemiologyProject ManagementEpidemiological MethodologiesFluent Professional English
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Pharmacoepidemiological Study DesignData AnalysisFeasibility StudiesLiterature ReviewsStatistical Analysis PlansHealth Database AnalysisStudy Protocol DevelopmentResults InterpretationQuality OversightBudget Management
Soft Skills
CommunicationCollaborationLeadership
Certifications & Qualifications
Master’s DegreePharmDMDPhD
Industry Keywords
Real-World DataObservational StudiesHealth DatabasesRegulatory RequirementsScientific Documentation
About the role
Key responsibilities & impact- Lead the operational and scientific execution of assigned Real-World Evidence (RWE) studies and projects
- Serve as the primary point of contact for internal teams and external stakeholders on RWE projects
- Design and implement pharmacoepidemiological studies using real-world data
- Provide methodological expertise on study designs, data sources, potential biases, and interpretation of results
- Conduct feasibility studies, literature reviews, and analyses of available health databases
- Oversee CROs and external partners, including protocols, deliverables, quality, budgets, and timelines
- Draft and review scientific documents, including protocols, statistical analysis plans, study reports, abstracts, publications, and presentations
- Contribute to the continuous improvement of standards and best practices
Requirements
What you’ll need- Master’s degree, PharmD, MD, or PhD in Epidemiology, Pharmacoepidemiology, Public Health, Biostatistics, or an equivalent scientific discipline
- Proven expertise in Real-World Evidence, pharmacoepidemiology, or applied epidemiology
- Experience designing and leading observational studies
- Expertise in RWE/RWD
- Project management skills and experience overseeing external partners
- Strong understanding of epidemiological methodologies, health databases, and related regulatory requirements
- Fluent professional English required
- Fluent professional French required
Benefits
Comp & perks- Inclusive, diverse, and equitable work environment
- Equal opportunity
- Professional development
- Diverse, high-impact projects
- Collaboration with recognized experts
- Integrated service model (Resourcing, Functional Service Provider, and Full Service)
- Contribution to improving the patient journey
