Descrizione:
Experteer OverviewIn this role you drive the operational management of assigned clinical projects, ensuring alignment with Chiesi’s goals and medical standards. You will coordinate with CROs, internal partners, and vendors to deliver studies on time and within budget. You’ll act as the primary operational contact for clinical trials and contribute to study design and risk management. This is an opportunity to shape multi-site trials in a global R&D environment and impact patient outcomes through rigorous study execution.Retribuzione / BenefitsCoordinate day-to-day operational management of 1–3 clinical trials, ensuring timelines and budgets are respectedAct as primary operational contact for CROs and internal stakeholders;
represent the Study Team for trial activitiesReview study documents from CROs (plans, risk, site contracts) and perform co-monitoring as neededMaintain Study Risk Register and drive follow-up actions with vendorsManage study eTMF with CTA and ensure compliance with SOPs and quality standardsPrepare and coordinate scientific meetings and expert/KOL contracts as requiredPrepare/review CSR and support presentation of results;
liaise with CTS on CTS strategy and executionEnsure budget planning and management for ongoing studiesResponsabilitàAt least 3 years of experience in a similar pharmaceutical roleTrack record of planning and executing 5+ clinical studiesDegree in Life Sciences or equivalentEnglish fluentKnowledge of clinical study design, Clinical Research Statistics, planning tools, ICH/GCP and SOPsGLP knowledge for bio-analytical assays (clinical pharmacology) and literature awarenessRequisiti fondamentaliHybrid and remote working optionsPensionPrivate medical insuranceWellbeing programmeFlexible benefits programmeTicket restaurant#J-18808-Ljbffr