Ph3Clinical Project Manager – Based in Rome (Sponsor dedicated) /h3 pThe IQVIA Clinical Functional Service Partnerships (Clinical FSP) department provides highly skilled professionals to client project teams to set up and execute clinical trials. This role works on diverse therapeutic areas. /p pbClinical Project Manager /b is an integral part of trial delivery, liaising with clinical teams to bring new drugs to market faster. They are responsible for project delivery, ensuring contractual requirements are met in accordance with SOPs, policies, and practices. The focus is on productivity, quality, and financial performance. /p h3Main Responsibilities /h3 ul liParticipate in bid defense presentations in partnership with Business Development; may lead presentations for smaller, less complex regional studies. /li liResponsible for delivery and management of smaller, less complex regional studies. /li liDevelop integrated study management plans with the core project team. /li liAccountable for the execution of clinical studies (or an assigned portion) per contract, optimizing speed, quality, and cost while ensuring consistent use of study tools, training materials, and compliance with standard processes. /li liSet objectives of the core project team according to contract, strategy, and approach, communicate and assess performance. /li liCollaborate with other functional groups to support milestone achievement and manage study issues and obstacles. /li liMonitor progress against contract and proactively present project information to internal and external stakeholders. /li liManage risk and contingencies proactively and lead problem‑solving and resolution efforts. /li liAchieve project quality by identifying quality risks and issues. /li liServe as primary or backup project contact with customers, owning the relationship with key contacts and liaising with IQVIA business development representatives. /li liEnsure the financial success of the project. /li liForecast and identify opportunities to accelerate activities and bring revenue forward. /li liIdentify changes in scope and manage change control process. /li /ul h3Required Skills And Qualifications /h3 ul liBachelor’s degree in Life Sciences. /li liMinimum 3 years of relevant experience, including 2 years of project management experience. /li liAdvanced knowledge of the job area, typically obtained through advanced education combined with experience. /li liProven work experience in a CRA role. /li liKnowledge of clinical trial conduct and application of regulatory requirements such as ICH GCP and relevant local laws. /li liTherapeutic area knowledge in Oncology. /li liComputer skills including Microsoft Word, Excel, and PowerPoint. /li liFluent in English and good knowledge of Italian, preferably at least C1 level. /li liEffective communication, organizational, and problem‑solving skills. /li liStrong leadership competencies and ability to establish and maintain effective working relationships. /li liWillingness to work hybrid in Rome with regular visits to the office (3 times a week). /li /ul h3Additional Information /h3 ul liSeniority level – Mid‑Senior level /li liEmployment type – Full‑time /li liJob function – Project Management and Information Technology /li liIndustry – Hospitals and Health Care /li /ul pIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. Learn more at /p /p #J-18808-Ljbffr