ppSelect how often (in days) to receive an alert: /ph3Clinical Research Associate CRA Supervisor EMEA (50/50) /h3pAs 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. /ppAt Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. /ph3bPosition Summary /b /h3pWe are looking for a highly motivated and experienced clinical research professional to join our Medical Affairs team in a unique hybrid role combining: /pullib50% Clinical Research Associate (CRA) responsibilities /b /li /ulpIn 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. /ppThis role is ideal for an experienced Senior CRA who enjoys mentoring others while remaining actively involved in study execution. /ph3As a Clinical Research Associate (50%) /h3pYou will be responsible for the execution of monitoring activities in accordance with MDR, ISO 14155, applicable regulations, and study requirements. /ppKey responsibilities include: /pulliConducting Site Qualification, Site Initiation, Routine Monitoring, and Close-Out Visits /liliPerforming Source Data Verification (SDV) and source document review /liliEnsuring protocol compliance and subject safety /liliTraining and supporting site personnel /liliManaging and maintaining Investigator Site Files (ISF) /liliSupporting Ethics Committee (EC) and National Competent Authority (NCA)



submissions /liliSupporting safety reporting activities /liliManaging study-related queries and follow-up actions /liliPreparing sites for audits and regulatory inspections /liliActing as the primary contact for assigned study sites /li /ulh3As a CRA Supervisor (50%) /h3pYou will lead and develop a team of CRAs across the EMEA region while ensuring high-quality monitoring delivery and compliance. /ppKey responsibilities include: /pulliLeading, coaching, mentoring, and developing CRAs /liliSupporting onboarding and training of new CRAs /liliEnsuring monitoring activities are conducted according to plans and procedures /liliSupporting resource and workload planning /liliMonitoring performance and quality metrics /liliEnsuring audit and inspection readiness /liliActing as a key interface between Clinical Operations, Quality, Safety, Data Management, and Project Management /li /ulh3bEducation / Experience Requirements /b /h3ulliDegree in Life Sciences, Nursing, Pharmacy, Medicine, Biology, or a related field /liliScientific understanding of clinical research and medical devices /li /ulh3bSpecialized Skills / Other Requirements /b /h3ulliMinimum 10 years of clinical monitoring experience /liliProven experience as a Senior CRA /liliExperience mentoring, training, or supervising CRAs /liliStrong knowledge of: /liliISO 14155 /liliMDR /liliClinical trial regulations and requirements /li /ulh3Technical Skills /h3ulliMicrosoft Office /lilieTMF /lilieCRF /liliCTMS /li /ulh3Language Requirements (Mandatory) /h3pTo support study sites and stakeholders across Europe, candidates must be fluent (written and spoken) in: /ppbAt least one Romance language, such as: /b /pulliFrench /liliSpanish /li /ulpApplications that do not meet all three language requirements cannot be considered.



/ph3What Makes You Successful /h3ulliStrong leadership and coaching skills /liliExcellent communication and stakeholder management /liliHigh attention to detail /liliStrong organizational skills /liliAbility to work independently and make sound decisions /liliCollaborative mindset with a focus on quality and compliance /liliPassion for developing people while driving operational excellence /li /ulh3Why Join Us? /h3pThis 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. /ppIf you are an experienced clinical research professional who enjoys both hands-on monitoring and people leadership, we would love to hear from you. /ppTeleflex 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. /ppIf you require accommodation and support to apply for a position, please contact us at /ppDiversity 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. /ppAt 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. /ppTeleflex, 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. /p /p #J-18808-Ljbffr

📌 Clinical Research Associate & CRA Supervisor EMEA (50/50) (Milano)
🏢 Teleflex
📍 Milano