Clinical Research Associate & Cra Supervisor Emea (50/50)
Pubblicato il 09-08-2026 - Teleflex in Bardi
ppSelect how often (in days) to receive an alert: /p h3Clinical Research Associate CRA Supervisor EMEA ******) /h3 pAs 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.
/p pAt Teleflex, we are empowering the future of healthcare.
For more information, please visit teleflex.com.
/p h3bPosition Summary /b /h3 pWe are looking for a highly motivated and experienced clinical research professional to join our Medical Affairs team in a unique hybrid role combining: /p ul lib50% Clinical Research Associate (CRA) responsibilities /b /li /ul pIn 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.
/p pThis role is ideal for an experienced Senior CRA who enjoys mentoring others while remaining actively involved in study execution.
/p h3As a Clinical Research Associate (50%) /h3 pYou will be responsible for the execution of monitoring activities in accordance with MDR, ISO *****, applicable regulations, and study requirements.
/p pKey responsibilities include: /p ul liConducting Site Qualification, Site Initiation, Routine Monitoring, and Close-Out Visits /li liPerforming Source Data Verification (SDV) and source document review /li liEnsuring protocol compliance and subject safety /li liTraining and supporting site personnel /li liManaging and maintaining Investigator Site Files (ISF) /li liSupporting Ethics Committee (EC) and National Competent Authority (NCA)
submissions /li liSupporting safety reporting activities /liliManaging study-related queries and follow-up actions /liliPreparing sites for audits and regulatory inspections /li liActing as the primary contact for assigned study sites /li /ul h3As a CRA Supervisor (50%) /h3 pYou will lead and develop a team of CRAs across the EMEA region while ensuring high-quality monitoring delivery and compliance.
/p pKey responsibilities include: /p ul liLeading, coaching, mentoring, and developing CRAs /li liSupporting onboarding and training of new CRAs /li liEnsuring monitoring activities are conducted according to plans and procedures /li liSupporting resource and workload planning /li liMonitoring performance and quality metrics /li liEnsuring audit and inspection readiness /li liActing as a key interface between Clinical Operations, Quality, Safety, Data Management, and Project Management /li /ul h3bEducation / Experience Requirements /b /h3 ul liDegree in Life Sciences, Nursing, Pharmacy, Medicine, Biology, or a related field /li liScientific understanding of clinical research and medical devices /li /ul h3bSpecialized Skills / Other Requirements /b /h3 ul liMinimum 10 years of clinical monitoring experience /li liProven experience as a Senior CRA /li liExperience mentoring, training, or supervising CRAs /li liStrong knowledge of: /li liISO ***** /li liMDR /li liClinical trial regulations and requirements /li /ul h3Technical Skills /h3 ul liMicrosoft Office /li lieTMF /li lieCRF /li liCTMS /li /ul h3Language Requirements (Mandatory) /h3 pTo support study sites and stakeholders across Europe, candidates must be fluent (written and spoken) in: /p pbAt least one Romance language, such as: /b /p ul liFrench /li liSpanish /li /ul pApplications that do not meet all three language requirements cannot be considered.
/p h3What Makes You Successful /h3 ul liStrong leadership and coaching skills /li liExcellent communication and stakeholder management /li liHigh attention to detail /li liStrong organizational skills /li liAbility to work independently and make sound decisions /li liCollaborative mindset with a focus on quality and compliance /li liPassion for developing people while driving operational excellence /li /ul h3Why Join Us?
/h3 pThis 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.
/p pIf you are an experienced clinical research professional who enjoys both hands?on monitoring and people leadership, we would love to hear from you.
/p pTeleflex 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.
/p pIf you require accommodation and support to apply for a position, please contact us at /p pDiversity 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.
/p pAt 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.
/p pTeleflex, 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.
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