ppBusiness Area: RD, Pharmacovigilance Regulatory Affairs /p pJob Type: Direct Employee /p pContract Type: Permanent /p pLocation: Italy, IT /p h3Responsibilities /h3 ul liEnd to end execution of assigned innovation and initiatives, translating strategies and study designs on time, quality, and compliant delivery across programs, therapeutic areas and geographies /li liAd hoc member of Integrated Clinical Teams, supporting cross functional alignment among Clinical Development, Clinical Evidence Epidemiology, Digital Health, Medical Affairs Patient Engagement /li liOperational planning, coordination and delivery of clinical innovation and real world evidence (RWE) projects on secondary data use, within the Global Clinical Development governance framework /li liExecute assigned clinical innovation, RWE, epidemiology, and database driven evidence projects in line with approved evidence strategies and pipeline priorities /li liTranslate approved concepts, protocols, and innovation designs into operational project plans, ensuring feasibility, scalability, and compliance /li liSupport implementation of approved innovation initiatives within ongoing development programs /li liParticipate in Integrated Clinical Team (ICT) activities for assigned programs, providing operational input and execution updates /li liSupport evidence and innovation decision making by translating strategic requirements into practical timelines, resource plans, and deliverables /li liEnsure coordination and information flow across involved functions and stakeholders /li liCoordinate and manage RWE studies and secondary data collection initiatives (regulatory and non regulatory) across the product lifecycle and geographies, under appropriate scientific oversight /li liSupport protocol development, study design finalization, and implementation of RWE studies in collaboration with Clinical Evidence Epidemiology and RWE leadership /li liEnsure operational control of timelines, quality,



and budget for assigned RWE projects /li liActs as connector and integration element between Global Medical Affairs and GCD /li liCoordinate cross functional study teams and external partners (CROs, data providers, registries, technology vendors) involved in innovation and RWE data driven initiatives /li liSupport vendor selection, onboarding, oversight, and performance monitoring in compliance with GCP, GVP, and applicable local regulations /li liAct as a day to day operational contact for vendors and service providers supporting assigned projects /li liSupport preparation, collection, and maintenance of study documentation required for Ethics Committees and Regulatory Authority submissions for RWE and innovation projects /li liEnsure appropriate eTMF set up, maintenance, quality checks, and reconciliation for assigned studies, including oversight of CRO filing activities /li liEnsure inspection ready documentation in alignment with internal standards and regulatory requirements /li liMonitor project budgets, invoices, and forecasts, ensuring alignment between contracted activities and actual costs /li liTrack milestones, risks, and dependencies, escalating issues as needed to ensure delivery commitments are met /li liProvide regular progress updates and performance reporting to project leadership and stakeholders /li liSupport the execution of digital health patient centric innovation initiatives, including pilots operational roll outs, in coordination with Clinical Digital Health Patient Engagement teams /li liEnsure integration of innovation outputs into ongoing clinical development and evidence programs /li liContribute to study results dissemination, scientific communications, and publications when required /li liSupport continuous improvement of innovation and RWE processes, tools,



and ways of working within the Clinical Innovation Unit /li liPromote consistent application of the 'framework and governance in place' aligned operational standards across projects /li /ul h3Qualifications /h3 ul liAt least 5 years of experience in biopharmaceutical industry in Evidence Generation or Clinical Operations Project management roles /li liMSc degree in scientific disciplines (Biology, Biotechnology, Chemistry, Pharmacy, Chemical and Pharmaceutical Technology) /li liProficiency in spoken and written English /li liExperienced in principles of study design, planning tools and principles /li liFamiliarity with the RWE/RWD regulatory framework, ICH/GCP and company SOPs /li liKnowledge of budget planning and administrative management /li liExperienced in documental archiving and management /li /ul h3Location /h3 pThe position is based at our headquarters in Parma and offers flexible working arrangements, including both hybrid and predominantly remote options. /p h3Compensation range /h3 pThe minimum salary for this role is €54.000, 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 h3Benefits /h3 pWe offer a comprehensive benefits package including pension, private medical insurance, wellbeing programme, flexible benefits programme, ticket restaurant and more. /p 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. This policy applies to all aspects of employment, including hiring, transfer, promotion, compensation, eligibility for benefits, and termination. /p /p #J-18808-Ljbffr

📌 Clinical Innovation Project Manager (Parma)
🏢 Chiesi Farmaceutici
📍 Parma