

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
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
משרות נוספות שיכולות לעניין אותך

Additional Locations: N/A
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.
(Senior) Specialist Health Economics & Market Access Rhythm Management DACH (m/w/d) Düsseldorf, hybrid
#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.
Zur Verstärkung unseres Rhythm Management (Cardiac Rhythm Management und Electrophysiology)-Teams suchen wir zum nächstmöglichen Zeitpunkt einen ambitionierten und motivierten (Senior) Specialist. Insbesondere durch unser sehr eindrucksvolles Produktportfolio, das unter anderem unser FARAPULSE™ PFA System beinhaltet, ist die Position sehr attraktiv.
(Senior) Specialist Health Economics & Market Access Rhythm Management DACH (m/w/d) im Büro in Düsseldorf, hybrid
Die Hauptaufgabe in dieser Position ist die Mitarbeit bei der Strategiedefinition, -entwicklung und Umsetzung. Sie arbeiten in der Abteilung HEMA (Health Economics & Market Access) für die DACH-Region und bringen Ihr Wissen über die Gesundheitssysteme und lokale Trends ein.
Im Fokus Ihrer operativen Tätigkeit steht die Schaffung von Möglichkeiten für die Kostenerstattung und den Marktzugang. Dies umfasst die Repräsentation von Boston Scientific bei relevanten Interessensgruppen (z. B. Regierungsstellen, Finanzierungs- und Kostenerstattungsgruppen, KOLs usw.) sowie die Anpassung bestehender gesundheitsökonomischer Modelle. Zudem arbeiten Sie mit lokalen Daten, um die kommerzielle Strategie zu stärken.
#Ihr Aufgabenbereich
· Entwicklung und Umsetzung von Strategien zur Sicherstellung einer optimalen Erstattung (Kodierung und Vergütung) für die Produkte und Verfahren von Boston Scientific
· Bewertung der Erstattungsmöglichkeiten und -herausforderungen für die innovativen und kommerziell vermarkteten Produkte des Unternehmens sowie Kommunikation der Auswirkungen
· Zielgerichtete Kommunikation der Erstattungsinformationen und Strategien an Marketing- und Vertriebsteams
· Durchführung von Datenbankanalysen (einschließlich DRGs), Marktanalysen und Literaturrecherchen sowie Präsentation gesundheitsökonomischer Ergebnisse vor internen und externen Stakeholdern
· Konzeption und Durchführung von internen und externen Schulungs- und Weiterbildungsmaßnahmen
· Überwachung politischer Entwicklungen, die potenziell die Erstattung von BSC-Produkten beeinflussen
· Identifikation, Aufbau und Pflege von Beziehungen zu Entscheidungsträgern (Gesundheitsbehörden, Krankenhäusern und Krankenkassen)
· Enge Zusammenarbeit mit funktionsübergreifenden Teams
· Vertretung von Boston Scientific auf Kongressen und Branchentreffen (z. B. BVMed)
#Ihr Kompetenzprofil
· Abschluss in Gesundheitsökonomie oder einem verwandten Bereich, idealerweise mit einer postgradualen Qualifikation in Gesundheitsökonomie.
· Mindestens 2 Jahre relevante Erfahrung im Bereich Marktzugang und/oder Gesundheitsökonomie, vorzugsweise in der Medizintechnik oder einem anderen relevanten Gesundheitssektor.
· Sehr gute Kenntnisse des Gesundheitssystems in Deutschland, Österreich und der Schweiz
· Eigenmotivierte, ergebnisorientierte Arbeitsweise und Anpassungsfähigkeit an neue Herausforderungen
· Ausgeprägte analytische Fähigkeiten
· Nachgewiesene Erfahrung im Projektmanagement
· Hohe soziale Kompetenz und Teamfähigkeit
· Ausgeprägte Kommunikations- und Überzeugungsstärke
· Fließende Deutsch- und Englischkenntnisse in Wort und Schrift
· Idealerweise Erfahrung in einem internationalen Konzernumfeld
· Reisebereitschaft (ca. 20 %)
#Unser Angebot
Neben einem spannenden Job, hoch innovativen Medizinprodukten und einem respektvollem Arbeitsumfeld in einem sympathischen Team bieten wir Ihnen u.a. ein leistungsgerechtes und attraktives Vergütungspaket sowie sehr gute Möglichkeiten zur persönlichen und fachlichen Entwicklung durch ein etabliertes Talentmanagement-Programm in unserer Organisation. Modernes IT-Equipment, betriebliche Altersvorsorge und weitere attraktive Sozialleistungen runden das Paket ab.
Vor allem bieten wir Ihnen aber eines: die Chance, Teil einer Unternehmenskultur zu werden, in der jeder seinen Beitrag dazu leistet, das Leben von Patienten besser zu machen. Wir freuen uns auf Ihre Bewerbung!
Boston Scientific Medizintechnik GmbH | Human Resources |
Klaus-Bungert-Straße 8 | 40468 Düsseldorf | www.bostonscientific.de
Requisition ID: 603892
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!
משרות נוספות שיכולות לעניין אותך

France-Île-de-France; Germany-Düsseldorf; Italy-Milan; United Kingdom-Hemel Hempstead
Salary:salary range depends on the country. For Italy and Spain, the range is approximately €50.000, - to €62.000, - excluding other benefits.
: in-depth understanding and expertise of pricing in a healthcare/MedTech setting, ideally on EMEA level. Strategic understanding/capabilities. Knows the type of stakeholders that you're dealing with and knowledge/understanding of market access & health economics based in either Madrid or Milan.
What your role will look like
You’ll be part of the RM EMEA Commercial & Customer Engagement (C&CE) team and report directly to our Pricing Lead RM EMEA. Working closely with theEMEA Pricing Center of Excellence, product management, and FP&A, you’ll bring clarity, insight, and consistency to our pricing strategy.
Here’s a glimpse of what you’ll be doing:
What you bring
You don’t need to be a pricing guru just yet but you do need the right mindset. If you're eager to learn, collaborate, and drive commercial impact, this role will offer the platform to grow. That said, you’ll likely thrive here if you:
What we offer you
We could talk about the salary, bonus, and benefits (and we will – transparently - during the process), but beyond that, we offer something more:
purpose, growth, and people.
Here’s what that looks like in practice:
משרות נוספות שיכולות לעניין אותך

This role consists of conducting confidential investigations involving conduct, discrimination, harassment, and retaliation in accordance with BSC policies, local laws, regulations, and requirements. This position also provides the opportunity to use consultative strategies while partnering with other peers and partners on escalations involving performance management, employee accommodations and sensitive employee situations. This position will support all functions in the EMEA region including Commercial Divisions, Global Operations, Global Functions and Global Supply Chain organizations.
Your responsibilities will include:
Other responsibilities:
Required Qualifications:
Other requirements:
משרות נוספות שיכולות לעניין אותך

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
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
משרות נוספות שיכולות לעניין אותך