Clinical Science Liaison Oncology jobs at Boston Scientific in Germany, Dusseldorf
Boston Scientific Clinical Science Liaison Oncology Germany, North Rhine-Westphalia, Dusseldorf
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France-Centre-Val de Loire; Italy-Milan; Spain-Madrid; United Kingdom-Hemel Hempstead
Key Responsibilities:
- Serve as a scientific and operational resource to clinical trial sites, supporting trial start-up, protocol education, and ongoing execution.
- Support patient treatment cases, as needed
- Provide expert input on site feasibility, patient recruitment strategies, and trial performance optimization.
- Act as a liaison between Boston Scientific and study sites, identifying and addressing factors impacting patient enrollment and data quality.
- Build strong peer-to-peer relationships with Key Opinion Leaders (KOLs) and provide clinical insights that inform both trial strategy and broader R&D activities.
- Collaborate closely with Medical Affairs and Clinical Operations teams to ensure synergy across clinical and educational engagements.
- Provide field intelligence and insights that influence study design, clinical development, and competitive positioning.
- Participate in clinical trial strategy development and contribute to shaping the future direction of IO&E research.
EDUCATION AND EXPERIENCE
- Bachelor’s degree required, terminal degree in clinically related area preferred (PharmD, PhD, MD/DO)
- Over 5 years experience functioning in an industry medical or clinical role supporting clinical trials.
- Track record for creating, managing and completing medical/scientific related projects.
- Oncology experience.
- Clinical trial acumen; preferably having clinical trial experience and knowledge of GCP
- Preferred experience
- Industry experience in a clinical, medical, or scientific liaison role
- Field experience
- Medical devices experience
SKILLS AND ATTRIBUTES
- Outstanding interpersonal consultative skills
- Excellent presentation/platform skills
- Detail oriented
- Self-motivated continuous scientific, technical and medical learning
- Ability to manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges
- Ability to creatively address problems in an organized systematic way
- Willingness and ability to work within and outside of traditional business hours
- Collaborative style, responsive, considerate, flexible, assertive and personable
- Strong knowledge of Microsoft Office Products and web based customer and clinical support tools
- Ability to operate a car and maintain a valid driver’s license
- Physical ability to operate interventional instrumentation
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Boston Scientific Sr Clinical Trial Manager Oncology Germany, North Rhine-Westphalia, Dusseldorf
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As part of the software development team, you will lead the creation of high-performance rendering and workflow tools. You will collaborate closely with hardware engineers, systems engineers, clinical teams, and field technicians to create cutting-edge tools for physicians and care teams. The role will involve full lifecycle software development, including requirements, architecture, design, implementation, and validation.
Your responsibilities will include:
Generate UI concepts and implement prototypes to gather user feedback on workflow and usability
Design and build elegant solutions for complex clinical problems in user interaction and visualization
Lead enhancements for real-time 3D rendering and advanced visualization technology
Collaborate effectively with hardware, systems, quality, and test teams to ensure end-to-end solution integrity
Participate in preclinical system experiments with physicians and third parties to evaluate system performance
Implement, test, troubleshoot, and debug source code for complex medical software applications
Drive software development through the full product lifecycle, including requirements, design, planning, code reviews, and documentation
Contribute to technical documentation such as design specifications, test plans, and user manuals
Foster a culture of pragmatic decision-making and cross-functional collaboration
Identify and drive continuous improvements in development tools and processes
Support field clinical staff with software use and issue troubleshooting
Required Qualifications:
BS or MS in Computer Science or a related field
Minimum of 5 years' experience in software development
Strong programming experience in C++
Experience with OpenGL and 3D graphics programming
Solid understanding of object-oriented programming principles
Excellent analytical and problem-solving skills
Demonstrated ability to understand user needs and design intuitive user interfaces
Ability to manage multiple projects in parallel
Experience with full software development lifecycle processes
Strong communication skills, both written and verbal
Preferred Qualifications:
Experience with Qt (QML is a plus)
Experience developing on Linux platforms
Familiarity with Agile and Scrum methodologies
Understanding of medical device standards such as IEC 62304, IEC 60601, ISO 14971, ISO 13485
Experience with software tools such as Git, Jira, and JAMA
Experience mentoring junior engineers
Quick learner with adaptability to master complex systems and new technologies
Working conditions:
Hybrid work model
Travel: 0–10%
Maximum Salary: $ 197000
Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
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Boston Scientific Field Clinical Specialist CRM m/w/d Germany, North Rhine-Westphalia, Dusseldorf
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DEIN VERANTWORTUNGSBEREICH
- Aktive Unterstützung bei Implantationen und bei Nachsorgeuntersuchungen von CRM-Produkten nach sorgfältiger Einarbeitung
- Ansprechperson für technische und produktbezogene Fragen
- Organisation und Durchführung von Kundentrainings und Kongressbesuchen
- Ausbau und Pflege unserer Kundenbeziehungen
- Unterstützung unseres Sales-Teams und der Studienabteilung
- Informationsaustausch mit dem Vertrieb und der Abteilung Customer Service
DEIN KOMPETENZPROFIL
- Erfolgreich abgeschlossenes Studium der Medizintechnik bzw. eines vergleichbaren Studiengangs oder eine erfolgreich abgeschlossene Ausbildung als Krankenschwester/-pfleger mit entsprechender Berufserfahrung
- Erste Berufserfahrung sowie fundiertes Fachwissen auf dem Gebiet der Medizintechnik
- Gute Kommunikationsstärke und Zuverlässigkeit
- Versierter Umgang mit dem MS Office-Paket
- Gute Englischkenntnisse in Wort und Schrift
- Hohe Mobilitäts- und Reisetätigkeit (Führerschein vorhanden) mit Wohnsitz im genannten Gebiet
- Start: Bei unserem „Welcome Days“ lernst Du uns besser kennen und knüpfst erste Kontakte
- Motivation: Du trägst täglich dazu bei, das Leben von Menschen zu verbessern
- Flexibilität : Du arbeitest zu 100% remote - vor Ort bei unseren Kunden und aus dem Home-Office
- Entwicklung & Wachstum: Durch Mentoring, Trainings und kontinuierliches Feedback wird's möglich
- Diversität & Gleichstellung: Leb` es mit uns und nehme teil an unsere Initiativen „EmpowHer“, „Pride“ und "FOAR"
- Gesundheit: Schwing Dich auf’s Jobrad und nutze Fitnessangebote über Gympass
- Firmenwagen: Mit Deinem Firmenwagen bleibst Du im Rollen – beruflich wie privat
- Gemeinsame Erfolge: AS ONE erzielen wir Erfolge, fördern Stärken, meistern Herausforderungen
Klaus-Bungert-Straße 8 | 40468 Düsseldorf |
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Boston Scientific Field Clinical Specialist Elektrophysiologie m/w/d Germany, North Rhine-Westphalia, Dusseldorf
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Your responsibilities will include:
- Oversee the Cryo Ablation product development organization and hold a key position on the franchise leadership team which oversees the ablation business within Interventional Oncology and Embolization.
- Develop best practices and establish expertise to support capital equipment development across franchises, supporting all Peripheral interventions.
- Creating and standardizing communication methodologies for cross-functional integrations, both within the project teams and to various stakeholder groups.
- Develop technology and exploratory roadmaps to support a long-term product development pipeline.
- Contribute to the organization’s vision by considering product development strategies and partnerships with global and local commercial and development teams.
- Develop extensive internal contacts across BSC and external contacts to facilitate strategic discussions and partnerships.
- Support and maintain expertise of applicable global development standards for both single use device and capital equipment.
- Anticipate changing demands, evaluate key business challenges, and develop innovative solutions affecting future strategies.
- Relationship/People Management: Directs and influences multiple cross-functional development teams; Provides input to functional directors on team and team member performance; Develops and maintains strong relationships with functional heads and Sr. Leadership to drive success of team. Actively influences cross-functional collaboration.
- Lead a diverse and global team of technicians, engineers, program managers and scientists through a team of direct leaders and be accountable for effective coaching and career development activities at all levels.
Required qualifications:
- Bachelor’s degree in engineering or applicable technical field.
- 12+ years' engineering or technical experience in the Product Life Cycle Process in the Medical Device industry.
- 5+ years' experience directly managing senior level leaders. Previous experience managing large global teams through their People Leaders.
- Highest ethical standards. Discretion and sound judgment when dealing with confidential and/or sensitive information.
- Travel may be required for up to 25% of the time.
Preferred qualifications:
- Advanced degree in engineering and/or management.
- Experience with (Single Use Devices) SUDs and Capital equipment.
- Ablation technology or Oncology product development experience.
- Strong collaboration skills.
Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
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Boston Scientific Senior Clinical Evaluation Scientist Germany, North Rhine-Westphalia, Dusseldorf
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Belgium-Diegem; France-Voisins le Bretonneux; Germany-Düsseldorf; Italy-Milan; Netherlands-Kerkrade; Spain-Madrid; United Kingdom-Hemel Hempstead
About the role:
This is a highly dynamic role in which you will work in a team environment to develop global evidence-based clinical strategies for cardiology medical devices (Cardiac Rhythm Management) by creating clinical documentation that systematically synthesizes information from multiple data sources. As a Clinical Evaluation Scientist, you will plan and develop clinical evaluation reports (CERs) and post-market clinical follow-up (PMCF) reports, as well as summary of safety and clinical performance reports (SSCPs) in alignment with applicable clinical and regulatory standards and business needs. This role applies analytical thought processes and a highly methodical clinical evaluation approach to develop benefit/risk profiles for the Boston Scientific portfolio cardiology devices. A successful candidate has excellent writing skills as well as the ability to work collaboratively with cross-functional partners. Your efforts support product approval, indication expansion and claim support, and mandated post-market requirements.
Your responsibilities will include:
Compile, appraise, and evaluate data from multiple sources including clinical trials, medical literature, design verification/validation data, and product complaint data. Compare and align this data with Risk Documentation and product labeling to identify gaps or emergent concerns.
Develop literature search strategies in collaboration with librarians and perform methodical evaluation of medical literature including screening, appraisal and extraction of relevant data.
Develop Clinical Benefit Statements in collaboration with medical experts and develop pre- and post-market data collection strategies to support the developed statements.
Create analyses to evaluate product benefit/risk profile, safety (e.g., develop a profile of adverse events), and performance. Identify potential clinical evidence gaps and contribute to development of prospective evidence strategy to address gaps.
Develop global clinical data strategies in collaboration with leadership and cross-functional partners to support market access for New Product Development, Sustaining Product compliance and Design Changes to existing products.
Manage ongoing Design and Quality activities to support necessary changes and/or improvements to devices, including assessing the impact to existing clinical data strategies, proposing and developing new clinical data activities to meet any identified gaps, and coordinating with management to ensure resourcing needs are considered.
Aid in the development and execution of strategies for responses for regulatory submissions.
Minimum Qualifications
Bachelor’s, Master’s or Advanced degree (PhD, research-based MS, MD, RN, DVM) in a scientific, medical, or engineering field.
6+ years professional experience in a scientific, engineering, medical, or medical device space
3+ years of experience inat least oneof the following: 1) Writing and Developing Clinical Evaluation Plans/Reports and Post-Market Clinical Follow-Up Plans/Reports in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations), relevant Medical Device Coordination Group (MDCG) guidance, and harmonized standards; 2) Working in the clinical treatment and management of patients receiving Cardiac Rhythm Therapies, including but not limited to: Pacemakers; Implantable Cardioverter-Defibrillators (ICDs); Cardiac Resynchronization Therapy Pacemakers/Defibrillators (CRT-P/Ds); or Subcutaneous Implantable Cardioverter Defibrillators (S-ICDs) or 3) Writing, Developing, Managing, and Submitting Regulatory Technical Documentation submissions in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations) to support EU Market access of Cardiac Rhythm Devices
Thorough understanding of different types of clinical evidence (e.g., literature, clinical trials, real-world evidence, etc.) and the benefits and limitations of each type of data.
Experience in strategically applying knowledge of regulations, medical knowledge, and data types to develop clinical data strategies to support submission.
Analytical skills, including strong familiarity with medical literature
Strong medical/scientific writing skills
- Advanced proficiency in English aligned with C1 level or 85-90% proficiency
Preferred Qualifications
3+ years of professional experience inmultipleof the areas identified above
Experience with/knowledge of with Quality Management System documentation, specifically Risk Management Documents (e.g., Hazard Analysis, Risk Management Report, Risk Management Plan)
Experience with engineering documentation, including test protocols, test reports, and international standards
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Boston Scientific Field Clinical Specialist- EP Germany, North Rhine-Westphalia, Dusseldorf
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Field Clinical Specialist Electrophysiology (FCS EP), you can be part of that change.
In this role, you'll support cardiologists and medical staff during advanced EP procedures and help shape the future of our electrophysiology portfolio. You’ll work with solutions like EP recording and pacing systems (LabSystemPro & MicroPace), diagnostic and therapeutic catheters (Blazer), Ultra-High-Density 3D mapping (OPAL HDx), and ablation therapies such as Cryoablation (POLARx) and Pulsed Field Ablation (Farapulse & Faraview). A background as a specialized nurse, electrophysiology technician, or clinical technologist (Technische Geneeskunde) will serve you well.
Your role as a Field Clinical Specialist EP in Germany
As FCS EP, you’re the go-to technical expert and clinical consultant for hospitals and physicians. You’ll support procedures, provide training, and play a key role in successful product implementation. Expect a dynamic field-based schedule—often you’ll only know the next day’s plan by the night before.
What you’ll be doing
- ✅Procedure & technical support – Provide hands-on support during ablation and other EP procedures. You’ll advise physicians on optimal system and catheter use.
- ✅Training & education – Train and guide cardiologists, electrophysiologists, and EP-lab staff in using our products—in the OR, and through structured sessions.
- ✅Relationship-building – Build trust-based relationships with medical professionals and make sure they’re always up to speed with the latest in EP.
- ✅Cross-functional collaboration – Work closely with Account Managers and Product teams to identify customer needs and market opportunities.
- ✅Clinical insights & innovation – Share feedback and insights with our R&D teams to contribute to product innovation and development.
A day in the life
Your day might start early with a hospital visit to support an ablation procedure. You’ll ensure all systems are ready and assist the clinical team in real time. In between procedures, you catch up with doctors or technicians to share clinical insights or discuss updates in our portfolio.
What you bring
You’ll likely tick one of the following boxes:
- 2–5 years of independent experience with 3D cardiac mapping or EP recording systems, OR
- 3–5 years of clinical experience in electrophysiology, OR
- 6–10 years of experience in a cardiology-related role
Bonus points for:
- Knowledge of the CRM/EP market
- Fluent German and English (a must for this role)
- Willingness to travel frequently within Germany
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Boston Scientific Field Clinical Specialist - Elektrophysiologie m/w/d Germany, North Rhine-Westphalia, Dusseldorf
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Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.
#Boston Scientific
Seit 40 Jahren arbeitet Boston Scientific als weltweit führendes Medizintechnikunternehmen an dem Ziel, das Leben von Patienten zu verbessern. Täglich stellen wir uns den wichtigsten Herausforderungen der Gesundheitsbranche mit innovativen Produkten, einer Kultur der Zusammenarbeit und einer tiefen Leidenschaft für die Verbesserung des menschlichen Lebens – das macht eine Karriere bei Boston Scientific zu mehr als nur einem Job. Wenn Sie ein Teil davon werden und Ihrer Berufung folgen möchten, dann sollten wir uns kennenlernen.
Für unser Außendienstteam im Bereich Elektrophysiologie (EP) suchen wir für einige regionen in Deitschland zum nächstmöglichen Zeitpunkt einen;
Field Clinical Specialist - Elektrophysiologie (m/w/d)
#Ihr Aufgabenbereich
- Aktive Unterstützung bei der Anwendung von EP-Produkten nach sorgfältiger Einarbeitung
- Ansprechperson für produktbezogene und medizintechnische Fragen
- Organisation und Durchführung von Kundentrainings und Kongressbesuchen
- Ausbau und Pflege unserer Kundenbeziehungen
- Unterstützung unseres Sales-Teams und der Studienabteilung
- Informationsaustausch mit dem Vertrieb und der Abteilung Customer Service
#Ihr Profil
- Eine erfolgreich abgeschlossene Ausbildung als Krankenschwester/-pfleger oder Kardiotechniker/in
- Idealerweise konnten Sie bereits erste praktische Erfahrungen durch Praktika und/oder Werkstudierendentätigkeiten sammeln
- Hohes Maß an sozialer Kompetenz und Teamfähigkeit
- Starke Kunden- und Patientenorientierung sowie Kontaktstärke und Zuverlässigkeit
- Gute Kenntnisse der englischen Sprache in Wort und Schrift
- Hohe Flexibilität vor allem im Sinne ausgeprägter Reisebereitschaft im jeweiligen Gebiet
Ihre Vorteile
- Start: Bei unserem „Welcome Days“ lernen Sie uns besser kennen und knüpfen erste Kontakte
- Motivation: Sie t ragen täglich dazu bei, das Leben von Menschen zu verbessern
- Flexibilität : Sie arbeiten zu 100% remote - vor Ort bei unseren Kunden und aus dem Home-Office
- Entwicklung & Wachstum: Durch Mentoring, Trainings und kontinuierliches Feedback wird's möglich
- Diversität & Gleichstellung: Leben Sie es mit uns und nehmen Sie teil an unsere Initiativen „EmpowHer“, „Pride“ und "FOAR"
- Firmenwagen: Mit Ihrem Firmenwagen bleiben Sie im Rollen – beruflich wie privat
- Gemeinsame Erfolge: AS ONE erzielen wir Erfolge, fördern Stärken, meistern Herausforderungen
Unsere Werte: Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
Wenn Sie Lust auf eine neue Herausforderung haben und ein wertvolles Teammitglied von Boston Scientific werden möchten, dann bewerben Sie sich mit Ihren vollständigen Bewerbungsunterlagen unter Angabe Ihrer Kündigungsfrist und Gehaltsvorstellung.
Wir freuen uns auf Sie!
Boston Scientific Medizintechnik GmbH | Human Resources | Codrina Schech
Klaus-Bungert-Straße 8 | 40468 Düsseldorf |
Unsere Karriereseite:
Wir beziehen uns auf alle biologischen Geschlechter und Geschlechtsidentitäten - wir hoffen, Sie fühlen sich angesprochen.
Requisition ID: 606509
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
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France-Centre-Val de Loire; Italy-Milan; Spain-Madrid; United Kingdom-Hemel Hempstead
Key Responsibilities:
- Serve as a scientific and operational resource to clinical trial sites, supporting trial start-up, protocol education, and ongoing execution.
- Support patient treatment cases, as needed
- Provide expert input on site feasibility, patient recruitment strategies, and trial performance optimization.
- Act as a liaison between Boston Scientific and study sites, identifying and addressing factors impacting patient enrollment and data quality.
- Build strong peer-to-peer relationships with Key Opinion Leaders (KOLs) and provide clinical insights that inform both trial strategy and broader R&D activities.
- Collaborate closely with Medical Affairs and Clinical Operations teams to ensure synergy across clinical and educational engagements.
- Provide field intelligence and insights that influence study design, clinical development, and competitive positioning.
- Participate in clinical trial strategy development and contribute to shaping the future direction of IO&E research.
EDUCATION AND EXPERIENCE
- Bachelor’s degree required, terminal degree in clinically related area preferred (PharmD, PhD, MD/DO)
- Over 5 years experience functioning in an industry medical or clinical role supporting clinical trials.
- Track record for creating, managing and completing medical/scientific related projects.
- Oncology experience.
- Clinical trial acumen; preferably having clinical trial experience and knowledge of GCP
- Preferred experience
- Industry experience in a clinical, medical, or scientific liaison role
- Field experience
- Medical devices experience
SKILLS AND ATTRIBUTES
- Outstanding interpersonal consultative skills
- Excellent presentation/platform skills
- Detail oriented
- Self-motivated continuous scientific, technical and medical learning
- Ability to manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges
- Ability to creatively address problems in an organized systematic way
- Willingness and ability to work within and outside of traditional business hours
- Collaborative style, responsive, considerate, flexible, assertive and personable
- Strong knowledge of Microsoft Office Products and web based customer and clinical support tools
- Ability to operate a car and maintain a valid driver’s license
- Physical ability to operate interventional instrumentation
These jobs might be a good fit
