RWE Strategy Lead - Real-World Evidence Expert

PIERRE FABRE; Asnières-sur-Seine; On-site; EUR 90,000 - 130,000; Full time

Job summary

Pierre Fabre Laboratories seeks a Real World Evidence Strategy Lead to shape the scientific strategy for RWE generation across products and indications. You will design observational studies, select data sources, and oversee analyses in collaboration with biostatisticians and cross‑functional teams.

The role requires leading RWE protocols, interpreting results in clinical and regulatory contexts, and communicating findings through publications and internal reports.

Qualifications

• Education aligned with epidemiology or public health; observational study experience required.
• Demonstrated ability to design, manage and interpret pharmacoepidemiology research.
• Experience leading observational protocols with regulatory considerations.

Responsibilities

• Define the scientific strategy for real-world evidence generation for products or programs.
• Lead methodological design of RWE studies from research question to final design.
• Identify relevant data sources and conduct FFPA assessments for data suitability.
• Ensure rigour of protocols and statistical analysis plans; mitigate biases.
• Interpret complex analyses and translate results into robust conclusions.
• Provide scientific support to operational teams and external partners.

Education

Master's degree or PhD in epidemiology, pharmacoepidemiology or public health, or medical doctor/pharmacist with significant observational study experience

Strong analytical and methodological skills in study design and interpretation

Lead Author experience for observational study protocols

Experience in comparative/regulatory-grade observational studies (EMA/FDA)

Experience with IEGP design and execution

Hands-on experience with real-world data sources (claims data)

Job description

Pierre Fabre Laboratories seeks a Real World Evidence Strategy Lead to shape the scientific strategy for RWE generation across products and indications. You will design observational studies, select data sources, and oversee analyses in collaboration with biostatisticians and cross‑functional teams.

The role requires leading RWE protocols, interpreting results in clinical and regulatory contexts, and communicating findings through publications and internal reports.