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Business Area: R&D;, Pharmacovigilance & Regulatory Affairs
Job Type: Direct Employee
Contract Type: Permanent
Location: Italy, IT
About us
Chiesi 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.
Chiesi Research & Development
Our R&D; team represents a fundamental asset for the business. It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery technology, clinical development, regulatory affairs, pharmacovigilance, intellectual property, quality assurance, R&D; project and portfolio management. Headquartered in the new purpose-built and fully integrated Research and Development Centre in Parma (Italy), the team also has important operations in Paris (France), Chippenham (UK), Cary (US), Stockholm (Sweden), Toronto (Canada) and Shanghai (China).
Who we are looking for
This is what you will do
End to end execution of assigned innovation and initiatives, translating straegies and study designs on time, quality, and compliant delivery across programs, therapeutic areas and geographies
Ad hoc member of Integrated Clinical Teams, supporting cross functional alignment among Clinical Development, Clinical Evidence & Epidemiology, Digital Health, Medical Affairs & Patient Engagement
You will be responsible for
Operational planning, coordination and delivery of clinical innovation and real world evidence (RWE) projects on secondary data use, within the Global Clinical Development governance framework
Execute assigned clinical innovation, RWE, epidemiology, and database driven evidence projects in line with approved evidence strategies and pipeline priorities
Translate approved concepts, protocols, and innovation designs into operational project plans, ensuring feasibility, scalability, and compliance




Support implementation of approved innovation initiatives within ongoing development programs
Participate in Integrated Clinical Team (ICT) activities for assigned programs, providing operational input and execution updates
Support evidence and innovation decision making by translating strategic requirements into practical timelines, resource plans, and deliverables
Ensure coordination and information flow across involved functions and stakeholders
Coordinate and manage RWE studies and secondary data collection initiatives (regulatory and non regulatory) across the product lifecycle and geographies, under appropriate scientific oversight
Support protocol development, study design finalization, and implementation of RWE studies in collaboration with Clinical Evidence & Epidemiology and RWE leadership
Ensure operational control of timelines, quality, and budget for assigned RWE projects
Acts as connector and integration element between Global Medical Affairs and GCD
Coordinate cross functional study teams and external partners (CROs, data providers, registries, technology vendors) involved in innovation and RWE data driven initiatives
Support vendor selection, onboarding, oversight, and performance monitoring in compliance with GCP, GVP, and applicable local regulations
Act as a day to day operational contact for vendors and service providers supporting assigned projects
Support preparation, collection, and maintenance of study documentation required for Ethics Committees and Regulatory Authority submissions for RWE and innovation projects
Ensure appropriate eTMF set up, maintenance, quality checks, and reconciliation for assigned studies, including oversight of CRO filing activities
Ensure inspection ready documentation in alignment with internal standards and regulatory requirements
Monitor project budgets, invoices, and forecasts, ensuring alignment between contracted activities and actual costs
Track milestones, risks, and dependencies, escalating issues as needed to ensure delivery commitments are met
Provide regular progress updates and performance reporting to project leadership and stakeholders
Support the execution of digital health & patient centric innovation initiatives, including pilots & operational roll outs, in coordination with Clinical Digital Health & Patient Engagement teams
Ensure integration of innovation outputs into ongoing clinical development and evidence programs
Contribute to study results dissemination, scientific communications, and publications when required
Support continuous improvement of innovation and RWE processes, tools,



and ways of working within the Clinical Innovation Unit
Promote consistent application of the 'framework and governance in place' aligned operational standards across projects
You will need to have
At least 5 years of experience in biopharmaceutical industry in Evidence Generation or Clinical Operations Project management roles
MSc degree in scientific disciplines (Biology, Biotechnology, Chemistry, Pharmacy, Chemical and Pharmaceutical Technology)
Proficiency in spoken and written English
Experienced in principles of study design, planning tools and principles
Familiarity with the RWE/RWD regulatory framework, ICH/GCP and company SOPs
Knowledge of budget planning and administrative management
Experienced in documental archiving and management
Location
The position is based at our headquarters in Parma and offers flexible working arrangements, including both hybrid and predominantly remote options.
Compensation range
The 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.
pension
private medical insurance
wellbeing programme
flexible benefits programme
tivcket restaurant
comprehensive healthcare programs
work-life balance initiatives
robust relocation support
What we offer
No 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.
Our salary package is competitive, comprising a basic salary, performance bonuses, and benefits benchmarked against the external market. Additionally, we offer flexible working arrangements, remote work options, and tax assistance services for foreign colleagues, all designed to help you thrive.
Chiesi 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. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination.
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📌 Clinical Innovation Project Manager (Lazio)
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