Senior Global Patient Safety Physician
Pubblicato il 29-08-2026 - Chiesi in Spoleto
ppSenior Global Patient Safety Physician Chiesi Poreta, Umbria, IT /p h3About us /h3 pChiesi is an international research-focused biopharmaceutical group with 90 years' experience, operating in more than 30 countries, with its Headquarter in Parma, Italy.
More than 8,000 employees across the group are united by a singular purpose: promoting a healthier world for our people, patients, and the planet.
This is what drives us as we research, develop, and market innovative drugs across our main therapeutic areas.
Discover more here.
At Chiesi we are thinking generations ahead, driving sustainable innovation with purpose.
This fosters a culture of reliability, transparency, and ethical behaviour at every level.
As a Benefit Corporation and a certified B Corp, we have embedded sustainability in our bylaws and continuously measure our impact.
Diversity and inclusion are at the heart of who we are.
We believe our differences make us stronger.
We are a vibrant ecosystem of passionate, talented individuals united by strong values, each bringing unique perspectives that help us to continuously challenge the status quo for the better.
/p h3This is what you will do /h3 ul liThe Senior Global Patient Safety Physician provides safety-scientific and medical expertise to the conduct of safety science activities and safety-related clinical development contributions for assigned development and marketed product(s).
/li liThis role requires medical and scientific leadership to ensure that the safety profiles of the concerned products are proactively monitored and assessed, using all available data sources.
/li liThe Senior Global Patient Safety Physician can be appointed as the safety science lead (as per the Safety Lead Role Card) to responsibly manage safety surveillance and risk management activities for assigned product(s) and ensure proactive, science-driven safety evaluation based on predictive safety strategies, robust surveillance, and informed benefit–risk decisions.
/li liYou will be responsible for provides safety-scientific and medical expertise to develop a Safety Science strategy and conduct safety surveillance and risk management activities for assigned development and marketed product(s).
/li liWorks in a fully integrated into a cross-functional context and deliver to the highest scientific and compliance standards.
/li liContributes to a forward-looking safety surveillance and risk management strategy for the assigned product(s) aligned with regulatory expectations and corporate priorities.
/li liEnsures continuous access to all relevant safety data to support the integrated oversight of emerging safety profiles across the assigned product(s).
/li liContributes to the evaluation of safety issues using all relevant data sources.
/li liCollaborates with stakeholders from Clinical Development, Medical Affairs, Regulatory Affairs, Quality,
and other functions in the context of the BRT.
/li liWorks with clinical teams to implement safety input into clinical development plans, protocols, study documents, and regulatory submissions.
/li liDevelops Health Hazard Assessments for quality complaints and manufacturing deviations, in line with the GMP quality process.
/li liDevelops the development of safety surveillance and risk management plans and other outputs for assigned product(s) as per relevant procedures, maintains the respective documentation and logs.
/li liMakes Safety Science contributions to due diligence, partnerships, licensing opportunities, and acquisition assessments.
/li liSupports the partner engagements for the continuous information exchange, as per the PV agreement.
/li liParticipates in the implementation of improvement initiatives to increase efficiency, quality, and scientific value within Safety Science activities.
/li liCollaborates with external providers managing outsourced activities for Patient Safety Science to ensure the communication flow for required data and the receipt and documentation of deliverables.
/li liCollaborates with Safety Operations on a day to day basis to have awareness of the flow of cases the coding and case quality.
/li liContributes to the development of safety communications material for global Health Authorities and external stakeholders.
/li liParticipates as subject matter expert during inspections, audits, and regulatory interactions, participating in remediation activities as required.
/li liParticipates in scientific development opportunities to strengthen expertise in safety assessment and methodology.
/li liParticipates in innovation and best practices in safety science to strengthen Chiesi's development and lifecycle management capabilities for the assigned products.
/li liSupports the engagement with external stakeholders, academic groups, and service providers to enhance scientific credibility and innovation.
/li liContributes to the integration of emerging science, regulatory trends, and best practices into Safety Science for the concerned product(s).
/li /ul h3Qualifications /h3 ul liMedical degree, preferably with experience in clinical practice.
/li liMinimum 5 years of experience as a safety physician in safety science within a pharmaceutical or CRO organization, with experience in post-marketing and clinical development safety.
/li liProven leadership of global teams and complex safety portfolios across early and late development and post-approval products.
/li liExpertise in global PV regulations, inspections, governance, and cross-functional collaboration.
/li liExperience across multiple product modalities (small molecules, biologics, drug/device combination products) and therapeutic areas.
/li liStrategic mindset with the ability to translate safety science into business and development decisions.
/li liStrong leadership and sound judgment, capable of managing complexity, risk, and critical issues.
/li liProven ability to influence senior stakeholders and collaborate effectively across matrix and cross-functional environments.
/li liExcellent communication, analytical, and organizational skills, combined with high ethical standards and a strong commitment to patient safety and quality.
/li /ul h3Location /h3 pEurope (flexible) – remote or hybrid /p h3Compensation range /h3 pThe minimum salary for this role is ******, aligned to our established salary framework.
The final offer will reflect the candidate's skills, experience, qualifications and internal equity considerations.
This role is eligible to participate in an annual premio scheme, subject to company and individual performance.
/p h3What we offer /h3 pWhat we offerNo matter where your path starts at Chiesi, it leads to inspiring possibilities.
Your future is our focus, and we are committed to nurturing your development in our dynamic, friendly environment with access to resources and training every step of the way.
We provide top-class benefits, including comprehensive healthcare programs, work-life balance initiatives, and robust relocation support.
Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive.
/p h3Benefits /h3 ul liCompany car /li liPension /li liPrivate medical insurance /li liWellbeing programme /li liFlexible benefits programme /li liComprehensive healthcare programs /li liWork-life balance initiatives /li liRobust relocation support /li liFlexible working arrangements /li liRemote work options /li liTax assistance services for foreign colleagues /li liOther benefits as outlined in the package /li /ul h3Equal Employment Opportunity /h3 pChiesi is an equal opportunity employer committed to hiring a diverse workforce at all levels of our business.
All qualified applicants receive consideration for employment based on attitude and merit, without regard to race, national origin, age, sex, religion, disability, sexual orientation, marital status, military status, gender identity or expression, or any other basis protected by applicable laws.
xlwpduy This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination.
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