bOverview /b pIn this role you coordinate the operational management of assigned clinical projects to advance Chiesi’s pipeline in line with medical standards. You act as the primary liaison to CROs, providers, and internal stakeholders, ensuring study quality, timelines, and budget adherence. You play a key part in study design input and risk management, supporting the execution and reporting of clinical data. This position offers exposure to a globally distributed RD team and meaningful impact on patient-focused drug development. /p bRetribuzione / Benefits /bullipension /liliprivate medical insurance /liliwellbeing programme /liliflexible benefits programme /lilirelocation support /liliremote work options /li /ul bResponsabilità /bulliManage 1–3 clinical trials depending on size and phase /liliOversee Clinical CROs/Providers and serve as primary contact for CROs and internal customers /liliEnsure adherence to scope, timelines, and budget /liliReview study documents (project plan, monitoring plan, risk management plan, site contracts)



and perform co-monitoring as needed /liliContribute to Study Risk Register and lead clinical risk reviews with cross-functional teams /liliOversee study eTMF with CTA and coordinate CTS strategy with CTS team /liliCoordinate preparation of experts/KOL contracts when applicable /liliPrepare and review CSR with Medical Writer; support external/internal presentation of results /liliLiaise with CTS for CTS strategy; manage CTS delivery at sites /liliEnsure SOP compliance and manage CAPA and follow-ups, including audits /liliProvide clinical operations input during study design and CPAC meetings /liliBudget preparation and management for ongoing studies /li /ul bRequisiti fondamentali /bulliAt least 3 years in a similar pharmaceutical role /liliTrack record of successful planning and execution of at least 5 clinical studies /liliDegree in Life Sciences or equivalent /liliEnglish fluent /liliKnowledge of clinical study design and biostatistics /liliFamiliar with planning tools and principles /liliKnowledge of ICH/GCP and company SOPs /liliKnowledge of GLP for bio-analytical assays (clinical pharmacology) /liliUp-to-date with relevant literature /li /ululliStrong communication and stakeholder management /liliCross-functional collaboration /liliAttention to detail and organizational skills /liliClinical trial management and CRO oversight /liliBudget management for clinical studies /liliStudy design principles and statistics /li /ul

📌 Senior Clinical Project Manager (Cremona)
🏢 Chiesi
📍 Cremona