Select how often (in days) to receive an alert:Scorra la pagina per visualizzare tutti i requisiti del lavoro e le responsabilità che i candidati selezionati dovranno assumersi.Clinical Research Associate & CRA Supervisor EMEA (50/50)As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.At Teleflex, we are empowering the future of healthcare. For more information, please visit .Position SummaryWe are looking for a highly motivated and experienced clinical research professional to join our Medical Affairs team in a unique hybrid role combining:50% Clinical Research Associate (CRA) responsibilitiesIn this position, you will not only perform hands-on monitoring activities for clinical studies but also provide leadership, coaching, and operational oversight for Clinical Research Associates across the EMEA region.This role is ideal for an experienced Senior CRA who enjoys mentoring others while remaining actively involved in study execution.As a Clinical Research Associate (50%)You will be responsible for the execution of monitoring activities in accordance with MDR, ISO 14155, applicable regulations, and study requirements.Key responsibilities include:Conducting Site Qualification, Site Initiation, Routine Monitoring, and Close-Out VisitsPerforming Source Data Verification (SDV) and source document reviewEnsuring protocol compliance and subject safetyTraining and supporting site personnelManaging and maintaining Investigator Site Files (ISF)Supporting Ethics Committee (EC) and National Competent Authority (NCA)



submissionsSupporting safety reporting activitiesManaging study-related queries and follow-up actionsPreparing sites for audits and regulatory inspectionsActing as the primary contact for assigned study sitesAs a CRA Supervisor (50%)You will lead and develop a team of CRAs across the EMEA region while ensuring high-quality monitoring delivery and compliance.Key responsibilities include:Leading, coaching, mentoring, and developing CRAsSupporting onboarding and training of new CRAsEnsuring monitoring activities are conducted according to plans and proceduresSupporting resource and workload planningMonitoring performance and quality metricsEnsuring audit and inspection readinessActing as a key interface between Clinical Operations, Quality, Safety, Data Management, and Project ManagementEducation / Experience RequirementsDegree in Life Sciences, Nursing, Pharmacy, Medicine, Biology, or a related fieldScientific understanding of clinical research and medical devicesSpecialized Skills / Other RequirementsMinimum 10 years of clinical monitoring experienceProven experience as a Senior CRAExperience mentoring, training, or supervising CRAsStrong knowledge of:ISO 14155MDRClinical trial regulations and requirementsTechnical SkillsMicrosoft OfficeeTMFeCRFCTMSLanguage Requirements (Mandatory)To support study sites and stakeholders across Europe, candidates must be fluent (written and spoken) in:At least one Romance language,



such as:FrenchSpanishApplications that do not meet all three language requirements cannot be considered.What Makes You SuccessfulStrong leadership and coaching skillsExcellent communication and stakeholder managementHigh attention to detailStrong organizational skillsAbility to work independently and make sound decisionsCollaborative mindset with a focus on quality and compliancePassion for developing people while driving operational excellenceWhy Join Us?This is a unique opportunity to combine operational clinical monitoring with leadership responsibilities, allowing you to directly influence study quality, team development, and patient outcomes across the EMEA region.If you are an experienced clinical research professional who enjoys both hands-on monitoring and people leadership, we would love to hear from you.Teleflex is an equal opportunity employer. Applicants will be considered without regard to age, gender, race, nationality, ethnicity, civil status, family status, sexual orientation, disability, religion and/or membership of the traveller community.If you require accommodation and support to apply for a position, please contact us at Diversity fosters innovative thinking and entrepreneurship and that’s what we are about at Teleflex. We trust and value our people and their diversity and we make it fun to work here. We are on a journey to ensure our workplaces mirror the patients we serve and the communities we operate in. Our approach is simple, we embrace everyone and want them to feel they belong here. We are building a culture where all employees can bring their best and unique selves to work. If that appeals to you, we would love to hear from you. Come join a company where diversity is sought out and inclusivity is how we progress.At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front. xysqume Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, QuikClot™, LMA™, Pilling™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.#J-18808-Ljbffr

📌 Clinical Research Associate & Cra Supervisor Emea (50/50) (Milano)
🏢 Teleflex
📍 Milano