Project Manager (Medical Devices)
Pubblicato il 02-10-2026 - ClinOpsHub in Brindisi
ppLocation : Mesagne (BR), Italybr/Working hours: Full-timebr/Contract : Employment contract under the Italian CCNL Commercio (starting from €24,000 gross annual salary). The contract type will be defined based on the selected candidate's experience. /p pClinOpsHub S.r.l., founded in **** by Stefano Lagravinese, is a Contract Research Organization (CRO) self-certified with AIFA since ****. /p pWe are a key player in the clinical research sector, providing services to pharmaceutical companies, clinical sites, laboratories, and other CROs, with a strong focus on quality, innovation, and professional growth. /p h3Role Objectives /h3 pThe selected candidate will be responsible for planning, coordinating, and overseeing clinical research projects on medical devices, ensuring compliance with timelines, budget, and applicable regulatory requirements. /p pThe primary objective of this role is to ensure effective project execution, mitigate operational risks, and maintain high-quality standards in the management of clinical studies involving medical devices. /p pPrevious experience in the creation and management of eCRFs is required. /p h3Key Responsibilities /h3 ul liOverall management of clinical projects on medical devices and projects handled by the Clinical Operations Department /li liCoordination of project team operational activities /li liPrimary point of contact for Sponsors and project stakeholders /li liMonitoring of timelines, project budget oversight,
and cost control /li liIdentification and management of project risks /li liSupport in study start-up activities /li liCoordination of communication across functions and involved resources /li liPreparation and facilitation of internal and external project meetings /li liSupport in deviation and CAPA management /li liPeriodic reporting on project progress /li /ul h3Requirements /h3 ul liDegree in a scientific field (e.g., Biotechnology, Pharmacy, Chemistry and Pharmaceutical Technology, Biomedical Engineering, or related) /li liAt least 1 year of experience in clinical trial management /li liProven experience in medical device projects /liliKnowledge of Good Clinical Practice (GCP) /li liUnderstanding of clinical trial management processes /li liExperience in project budget and timeline management /li liFamiliarity with project risk management /li liExcellent command of English /li /ul h3What we offer /h3 ul liContinuous training and mentoring by senior professionals /li liCareer growth opportunities in a young and dynamic environment /li liPossibility of hybrid working arrangements /li liCompany benefits (welfare, meal vouchers, team building activities) /li /ul pThis job posting is open to candidates of all genders, ages, and nationalities (Italian Legislative Decree ******** and Directive *******/EC). /p pClinOpsHub actively promotes diversity: equal qualifications considered, priority may be given to candidates from underrepresented groups within the team. /p h3Privacy /h3 pPersonal data will be processed in accordance with Regulation (EU) ******** (GDPR) and applicable data protection laws. /p /p #J-*****-Ljbffr