Senior Global Patient Safety Physician

Overview As Senior Global Patient Safety Physician at Chiesi, you lead safety science for assigned products, shaping proactive risk management and safety surveillance. You collaborate across Clinical Development, Medical Affairs, Regulatory, Quality and external partners to integrate safety data into development plans and submissions. You drive science-led...

Chiesi Farmaceutici S.p.A. in Italy is seeking a Senior Global Patient Safety Physician to lead safety science activities and contribute to developing safety strategies for clinical products. The role demands a comprehensive understanding of safety regulations and the ability to oversee complex safety portfolios.The ideal candidate should have a medical...

Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, remote, IT About the role The Senior Global Patient Safety Physician provides safety-scientific and medical expertise to the conduct of safety science activities and...

GRAPS Patient Safety Operations, Post Marketing Manager Date: 26 Sept 2026 Department: Global Regulatory Affairs & Patient Safety Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Europe, remote, IT About us Chiesi is an international research-focused biopharmaceutical group with 90...

Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards.In this home-based role, you will coordinate monitoring...

Chiesi Farmaceutici S.p.A. in Parma is seeking a GRAPS Patient Safety Operations, Post Marketing Manager to lead post-marketing pharmacovigilance operations across our global portfolio, ensuring data quality, compliance and inspection readiness.The role collaborates with international stakeholders, oversees PV activities with CROs and PV service providers,...

Trial Form Support is seeking a remote Clinical Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance. You will coordinate monitoring activities, manage documentation, and participate in audits while supporting study conduct within a global, collaborative team.The role requires a Bachelor's in...

Overview In this home-based role, you will monitor clinical trials in oncology across sites, ensuring patient safety, data integrity, and regulatory compliance. You'll work within the Strategic Resourcing Solutions team to support study conduct, site management, and quality by adhering to GCP/ICH and SOPs. You'll coordinate monitoring activities, manage...

Overview In this role you steer the global clinical development strategy for key respiratory indications, leading a physician-scientist team across geographies. You will align R&D and commercial goals, shape trial designs, and drive regulatory success with high scientific and operational impact. You thrive in a cross-functional, matrix environment and help...