Director Real World Evidence Scientist (Oncology) (all genders)
Core
Own and drive end-to-end Real-World Evidence (RWE) strategy for complex oncology programs, integrating RWE into clinical development and regulatory strategies.
Role type
Director, Real-World Evidence Scientist (Oncology)
Builds
End-to-end RWE strategies and non-interventional studies for oncology drug development programs.
Domain
Healthcare / Life Sciences / Oncology
Required skills
RWE strategy design, non-interventional study management, secondary data analysis (claims, EMR, registries), federated data networks, OMOP CDM, FHIR, epidemiology, pharmacology, pharmacovigilance, regulatory/payer submissions, scientific mentorship
Preferred skills
AI/ML applications in RWE (NLP), patient-reported outcomes (PRO), health technology assessment, thought leadership via publications
Technologies
OMOP CDM, FHIR, claims data, electronic medical records, registries
Responsibilities
Define and lead RWE integration into clinical and regulatory strategies; design and oversee non-interventional studies from protocol to reporting; represent the organization with health authorities; contribute to peer-reviewed publications and conference presentations; champion methodological innovation and process improvements; mentor colleagues within the function
Seniority
Director, strategic leadership & mentorship
