Global Real-World Evidence Lead, Endo-Metabolic

Chiesi Farmaceutici S.p.A.; Parma; On-site; EUR 73,008 - 89,233; Full time

Benefits offered by this job

Annual bonus eligibility

Private medical insurance

Wellbeing programme

Flexible benefits

Relocation support

Job summary

Chiesi Farmaceutici S.p.A. is seeking a Real World Evidence Lead Endo-Metabolic to drive the global RWE strategy for the Endo‑Met portfolio within GRD.

You will shape the integrated evidence plan, align with cross‑functional teams, and advance innovative methodologies for regulatory and payer decision‑making. The role requires deep expertise in epidemiology, RWE, and real‑world data sources, with a track record of influencing senior stakeholders and leading complex studies across multiple

Qualifications

• Advanced degree in a relevant field (e.g., PhD, DrPH, MD, PharmD, MSc).
• 8+ years of experience in RWE, HEOR, epidemiology, or observational research in pharma/biotech.
• Proven track record in leading RWE strategy at asset or portfolio level.
• Strong experience with real‑world data sources (claims, EHR, registries).
• Ability to translate evidence into business and clinical impact.

Responsibilities

• Lead the global RWE strategy for the Endo‑Met GRD portfolio across development, regulatory, and commercialization phases.
• Oversee external data partnerships, due diligence, and governance of data sources.
• Foster scientific leadership in observational research, epidemiology, and RWE methodologies.
• Drive adoption of AI/ML and advanced analytics in RWE generation.
• Represent Chiesi externally in scientific forums and publications.

Skills

RWE leadership

Cross-functional leadership

Epidemiology

Real‑world data

AI/ML in RWE

Stakeholder influence

Regulatory & market access

Education

Advanced degree

Tools

AI/ML tools

EHR/Claims data systems

Data governance

Job description

Chiesi Farmaceutici S.p.A. is seeking a Real World Evidence Lead Endo-Metabolic to drive the global RWE strategy for the Endo‑Met portfolio within GRD.

You will shape the integrated evidence plan, align with cross‑functional teams, and advance innovative methodologies for regulatory and payer decision‑making. The role requires deep expertise in epidemiology, RWE, and real‑world data sources, with a track record of influencing senior stakeholders and leading complex studies across multiple