Kaufmann/-frau - Einzelhandel (Medizintechn./Sanitätsfach.)

Renal Denervation therapy is a vital component of the Interventional Cardiology Therapies (ICT) at Medtronic. In addition to products that support the diagnosis and treatment of coronary artery disease and the restoration of structural heart functions, we also are leading the way with the transformational renal denervation therapy, which has the potential to be a powerful tool in battling the global hypertension epidemic. It's no accident - we work hard to cultivate a workforce that reflects our patients and partners. We believe it's the only way to drive healthcare forward and remain a global leader in medical technology and solutions.

Location: remote position in Netherland, Belgium, Germany, United Kingdom or Austria

Ability to travel up to 75% primarily within Europe

Responsibilities may include the following and other duties may be assigned:

* Provides field support for various clinical research studies by selecting sites, performing activation duties, setting up protocols, providing training, helping to enroll participants, supporting cases, ensuring quality data acquisition and performing study closure activities

* Addressing clinical research site needs by maintaining frequent contact via email/phone/on-site visits with principal investigators, sub-investigators, and research coordinators

* Responsible for gaining and maintaining knowledge of clinical sites in a given geographic area to best understand and assess investigators' interests and capabilities

* Provides continuous communication to in-house clinical trial leaders regarding the status and performance of multiple studies

* Assist in control of device allocation, distribution and reconciliation

* Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies

* Interface with representatives from key functional groups (Monitoring, Data Management, Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and Clinical groups)

* Identify and mitigate quality risks and issues for assigned clinical studies, with oversight from study management. Oversee follow-up and resolution of site issues

* Refer to Standard Operating Procedures (SOPs) and study management process for guidance on everyday study tasks

* Participate in training to enhance knowledge base

* Assist with oversight of activities performed by Contract Research Organizations (e.g., CROs, core labs)

Required Knowledge and Experience:

* Bachelor's degree with 4 years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience - OR - Advanced degree with 2 years of clinical research/clinical (e.g. field clinical research/clinical specialist/field clinical engineer) experience

* Fluent in English, with excellent written and verbal communication skills; proficiency in additional European languages is preferred

* Good prioritization and organizational skills

* Problem-solving skills with attention to detail and accuracy

* Proficient in Microsoft Office, particularly Outlook, Excel, Word, and PowerPoint

Ideally, you bring:

* Experience with clinical/medical devices, preferably in catheterization labs, biomedical engineering or a hospital setting

* Background in cardiovascular/cardiac rhythm management devices or medical sales

* Experience in the medical device industry, clinical studies

* Strong collaboration skills with physicians, customers and cross-functional clinical stakeholders

* Knowledge of GCP and clinical trial regulatory requirements

* A clinical research certification (e.g. CCRP, CCRC) is a plus

Bewerben Sie sich bitte ausschließlich über unser Jobportal:https://medtronic.wd1.myworkdayjobs.com/de-DE/MedtronicCareers/job/Senior-Field-Clinical-Research-Specialist_R74167?locationCountry=d004c0d1a6c84511ab048669fcdf9fd7

Medtronic Österreich GmbH, Handelskai 94-96, 1200 Wien, https://www.medtronic.com/at-de/index.html