Expected Travel
: More than 50%
Requisition ID
: *****
About Teleflex Incorporated
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.
Teleflex is the home of ArrowTM, BarrigelTM, DeknatelTM, LMATM, PillingTM, QuikClotTM, RüschTM, UroLiftTM and WeckTM – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
Position Summary
We are looking for a highly motivated and experienced clinical research professional to join our Medical Affairs team in Austria in a unique hybrid role combining:
50% Clinical Research Associate (CRA) responsibilities
50% CRA Supervisor responsibilities
In 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.
Principal Responsibilities
As a Clinical Research Associate (50%)
You will be responsible for the execution of monitoring activities in accordance with MDR, ISO *****, applicable regulations, and study requirements.
Key Responsibilities Include:
Conducting Site Qualification, Site Initiation, Routine Monitoring, and Close-Out Visits
Performing Source Data Verification (SDV) and source document review
Ensuring protocol compliance and subject safety
Training and supporting site personnel
Managing and maintaining Investigator Site Files (ISF)
Supporting Ethics Committee (EC) and National Competent Authority (NCA) submissions




Supporting safety reporting activities
Managing study-related queries and follow-up actions
Preparing sites for audits and regulatory inspections
Acting as the primary contact for assigned study sites
As 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 CRAs
Supporting onboarding and training of new CRAs
Ensuring monitoring activities are conducted according to plans and procedures
Supporting resource and workload planning
Monitoring performance and quality metrics
Ensuring audit and inspection readiness
Acting as a key interface between Clinical Operations, Quality, Safety, Data Management, and Project Management
Education / Experience Requirements
Degree in Life Sciences, Nursing, Pharmacy, Medicine, Biology, or a related field
Scientific understanding of clinical research and medical devices
Specialized Skills / Other Requirements
Minimum 10 years of clinical monitoring experience
Proven experience as a Senior CRA
Experience mentoring, training, or supervising CRAs
Strong knowledge of:
ISO *****
MDR
Clinical trial regulations and requirements
Technical Skills
Microsoft Office
eTMF
eCRF
CTMS
Language Requirements (Mandatory)
To support study sites and stakeholders across Austria and Switzerland, candidates must be fluent (written and spoken) in:
English
German
At Least One Romance Language, Such As:
French
Italian
Spanish
Applications that do not meet all three language requirements cannot be considered.
What Makes You Successful
Strong leadership and coaching skills
Excellent communication and stakeholder management
High attention to detail




Strong organizational skills
Ability to work independently and make sound decisions
Collaborative mindset with a focus on quality and compliance
Passion for developing people while driving operational excellence
Why 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.
Teleflex, the Teleflex logo, ArrowTM, BarrigelTM, DeknatelTM, QuikClotTM, LMATM, PillingTM, RüschTM, UroLiftTM and WeckTM are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© **** Teleflex Incorporated. All rights reserved.

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