Clinical Innovation & RWE Project Lead

Chiesi; Cagliari; In loco; EUR 70.000 - 110.000; Tempo pieno

Vantaggi offerti da questo lavoro

Pension

Private medical insurance

Descrizione del lavoro

Chiesi in Sardegna is seeking a Clinical Innovation Project Manager to lead end-to-end RWE and evidence generation across geographies. You will translate strategies into actionable plans, ensure quality, compliance, and timely delivery, and collaborate with Global Clinical Development and Medical Affairs.

You will manage study design input, budget, timelines, and vendor oversight, apply GCP/GVP standards, and drive continuous improvement in RWE methods.

Competenze

• MSc degree in scientific disciplines and 5+ years in biopharma or related Evidence Generation/Clinical Operations.
• Experience with study design, planning tools and regulatory frameworks (ICH/GCP).
• Budget planning and administrative management experience.
• Strong communication and stakeholder management across cross-functional teams.

Mansioni

• Plan, coordinate and deliver clinical innovation and RWE projects within governance frameworks.
• Operate on RWE, epidemiology, and database-driven evidence projects aligned with approved strategies.
• Translate concepts into actionable project plans with feasibility and scalability in mind.
• Support implementation of approved innovation initiatives within development programs.
• Coordinate RWE studies and data collection across product lifecycles and geographies.
• Maintain timelines, quality, and budget controls for RWE projects.
• Prepare and maintain study documentation for Ethics Committees and Regulatory submissions.

Conoscenze

Cross-functional collaboration

Project management

Budget planning and administrative

Strong communication and stakeholder

RWE methodologies

Formazione

MSc degree in scientific disciplines (Biology, Biotechnology, Chemistry, Pharmacy, Chemical and Pharmaceutical Technology)

Descrizione del lavoro

Chiesi in Sardegna is seeking a Clinical Innovation Project Manager to lead end-to-end RWE and evidence generation across geographies. You will translate strategies into actionable plans, ensure quality, compliance, and timely delivery, and collaborate with Global Clinical Development and Medical Affairs.

You will manage study design input, budget, timelines, and vendor oversight, apply GCP/GVP standards, and drive continuous improvement in RWE methods.