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דרושים Senior Clinical Evaluation Scientist ב-Boston Scientific ב-Germany, Dusseldorf

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Senior Clinical Evaluation Scientist ב-Germany, Dusseldorf והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו Boston Scientific. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Germany
Dusseldorf
נמצאו 15 משרות
Yesterday
BS

Boston Scientific Clinical Science Liaison Oncology Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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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Yesterday
BS

Boston Scientific Senior Data Platform & MLOps Engineer EMEA - Dusseldorf Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
Backlog ownership & delivery: Convert outcomes into prioritized epics/stories, lead refinement and planning, uphold DoR/DoD, balance features with reliability, observability, cost, and sustainability. Value & metrics: Establish VIPs/KPIs/OKRs (adoption, time‑to‑data,...
תיאור:

ADay in the Lifeof the EMEA AI Product Owner:

You’ll begin your day translating business needs into technical requirements, prioritizing features in the backlog, and overseeing the AI product lifecycle to ensure successful, ethical, and valuable implementations. Key responsibilities include defining success criteria, collaborating with data scientists and engineers, and bridging the gap between business goals and AI capabilities.

You will work on initiatives like AgentForce AI, PACE and other new AI opportunities in the region.

You will collaborate with the AI Product Managers, Data Engineering, Platform, Architecture, and Governance teams to clarify data contracts, schemas, lineage, and access models, ensuring each increment is production-ready and guided by design. You’ll groom the roadmap and write user stories to add to the backlog, break down epics, refine acceptance criteria, and balance new features with technical debt, observability, and cost efficiency. You’ll demo recent increments, gather user feedback, and turn it into testable stories that enhance usability, trust, and performance. You’ll brief sponsors on the value delivered and present investment options for the next phases.

Your role is more technically demanding, requiring an understanding of AI technologies and ethical considerations. You must navigate challenges like data privacy and compliance with data protection regulations. Additionally, you will manage AI bias by providing diverse datasets for model training and using bias detection mechanisms to monitor AI outputs.

On a monthly rhythm, you’ll coordinate with global data and architecture forums to reuse patterns, converge on standards, and ensure EMEA needs are represented in the enterprise roadmap.

As a champion of the data strategy & enablement team, you will drive adoption through excellent product experience - discoverability in the catalog, clear documentation, and dependable service levels that help teams selfserve trustworthy, governed data at scale.


The role:

Reporting to the Product Ownership Sr Manager, the EMEA AI Product Owner is accountable for the dayday delivery of data products

You will translate business outcomes into product capabilities, manage scope and trade

Success requires a blend of AI technology expertise, stakeholder leadership, and hands-on ownership to deliver secure, compliant solutions for the EMEA region.

Key Responsibilities:

  • Backlog ownership & delivery: Convert outcomes into prioritized epics/stories, lead refinement and planning, uphold DoR/DoD, balance features with reliability, observability, cost, and sustainability.
  • Value & metrics: Establish VIPs/KPIs/OKRs (adoption, timetodata, data trust, NPS, ROI); run quarterly value reviews, iterate the roadmap based on evidence.
  • Privacy and Data Governance by design: Embed privacy, security, quality, and lifecycle controls (policies, lineage, access models, retention, auditability) into every increment, ensure GDPR compliance and data residency adherence.
  • Platform leverage & reusability: Reuse enterprise platforms, patterns, and reference architectures, drive reusability and scale across markets while meeting countryspecific requirements.
  • Stakeholder & change leadership: Communicate clearly at all levels; manage dependencies and risks, prepare business cases, Investment Board inputs, release notes, and adoption communications.
  • Incident, risk & release management: Triage issues, lead RCA, and prioritize preventative fixes, plan releases and change controls, coordinate rollbacks/hotfixes where needed.
  • Enablement & adoption: Publish documentation, examples, and learning paths, champion catalog discoverability, access requests, and community channels.
  • Financial stewardship: Own product budgets/forecasts, track benefits realization and ROI, report performance and outcomes to sponsors and Finance partners.
  • Global alignment: Partner with global product, platform, and architecture teams to align roadmaps, share learnings, and represent EMEA needs and impact.

What you will need:

  • Bachelor’s in Business, Computer Science, Engineering, or related field.
  • 7–10+ years across product management/ownership, data platforms, analytics, or digital strategy. Experience in medtech, pharma/consulting is a plus.
  • Strong understanding of AI, machine learning, and data science concepts. Proven success delivering AI products from concept to scaled adoption. Strong understanding of ethical AI considerations.
  • Excellent communication and collaboration skills.
  • Experience in defining product roadmaps and requirements.
  • Familiarity with AI tools and a data-driven approach.
  • Strong grasp of data privacy (GDPR), regulatory frameworks, security, and AI ethics.
  • Expert backlog management, story writing, acceptance testing, and agile delivery at scale (Scrum/Kanban).
  • Excellent communication and facilitation, able to influence executive, technical, and nontechnical audiences.
  • Technical fluency and eagerness for continuous learning in Data & AI capabilities and products.

What do you offer:

  • Ownership mindset with high accountability for user satisfaction and product reliability.
  • • Pragmatic product instincts: you simplify, focus, and drive value creation and delivery of AI products
  • • Learning agility and curiosity about emerging capabilities and responsible ways to apply them.

What do we offer:

  • A chance to drive innovation by delivering meaningful AI solutions across the EMEA region.
  • A collaborative, global network and supportive coaching culture focused on your growth.
  • Opportunities to lead high
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משרות נוספות שיכולות לעניין אותך

Yesterday
BS

Boston Scientific Sr Clinical Trial Manager Oncology Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
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...
תיאור:


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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משרות נוספות שיכולות לעניין אותך

Yesterday
BS

Boston Scientific Senior EMEA AI Product Owner - Düsseldorf Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
Backlog ownership & delivery: Convert outcomes into prioritized epics/stories, lead refinement and planning, uphold DoR/DoD, balance features with reliability, observability, cost, and sustainability. Value & metrics: Establish VIPs/KPIs/OKRs (adoption, time‑to‑data,...
תיאור:

ADay in the Lifeof the EMEA AI Product Owner:

You’ll begin your day translating business needs into technical requirements, prioritizing features in the backlog, and overseeing the AI product lifecycle to ensure successful, ethical, and valuable implementations. Key responsibilities include defining success criteria, collaborating with data scientists and engineers, and bridging the gap between business goals and AI capabilities.

You will work on initiatives like AgentForce AI, PACE and other new AI opportunities in the region.

You will collaborate with the AI Product Managers, Data Engineering, Platform, Architecture, and Governance teams to clarify data contracts, schemas, lineage, and access models, ensuring each increment is production-ready and guided by design. You’ll groom the roadmap and write user stories to add to the backlog, break down epics, refine acceptance criteria, and balance new features with technical debt, observability, and cost efficiency. You’ll demo recent increments, gather user feedback, and turn it into testable stories that enhance usability, trust, and performance. You’ll brief sponsors on the value delivered and present investment options for the next phases.

Your role is more technically demanding, requiring an understanding of AI technologies and ethical considerations. You must navigate challenges like data privacy and compliance with data protection regulations. Additionally, you will manage AI bias by providing diverse datasets for model training and using bias detection mechanisms to monitor AI outputs.

On a monthly rhythm, you’ll coordinate with global data and architecture forums to reuse patterns, converge on standards, and ensure EMEA needs are represented in the enterprise roadmap.

As a champion of the data strategy & enablement team, you will drive adoption through excellent product experience - discoverability in the catalog, clear documentation, and dependable service levels that help teams selfserve trustworthy, governed data at scale.


The role:

Reporting to the Product Ownership Sr Manager, the EMEA AI Product Owner is accountable for the dayday delivery of data products

You will translate business outcomes into product capabilities, manage scope and trade

Success requires a blend of AI technology expertise, stakeholder leadership, and hands-on ownership to deliver secure, compliant solutions for the EMEA region.

Key Responsibilities:

  • Backlog ownership & delivery: Convert outcomes into prioritized epics/stories, lead refinement and planning, uphold DoR/DoD, balance features with reliability, observability, cost, and sustainability.
  • Value & metrics: Establish VIPs/KPIs/OKRs (adoption, timetodata, data trust, NPS, ROI); run quarterly value reviews, iterate the roadmap based on evidence.
  • Privacy and Data Governance by design: Embed privacy, security, quality, and lifecycle controls (policies, lineage, access models, retention, auditability) into every increment, ensure GDPR compliance and data residency adherence.
  • Platform leverage & reusability: Reuse enterprise platforms, patterns, and reference architectures, drive reusability and scale across markets while meeting countryspecific requirements.
  • Stakeholder & change leadership: Communicate clearly at all levels; manage dependencies and risks, prepare business cases, Investment Board inputs, release notes, and adoption communications.
  • Incident, risk & release management: Triage issues, lead RCA, and prioritize preventative fixes, plan releases and change controls, coordinate rollbacks/hotfixes where needed.
  • Enablement & adoption: Publish documentation, examples, and learning paths, champion catalog discoverability, access requests, and community channels.
  • Financial stewardship: Own product budgets/forecasts, track benefits realization and ROI, report performance and outcomes to sponsors and Finance partners.
  • Global alignment: Partner with global product, platform, and architecture teams to align roadmaps, share learnings, and represent EMEA needs and impact.

What you will need:

  • Bachelor’s in Business, Computer Science, Engineering, or related field.
  • 7–10+ years across product management/ownership, data platforms, analytics, or digital strategy. Experience in medtech, pharma/consulting is a plus.
  • Strong understanding of AI, machine learning, and data science concepts. Proven success delivering AI products from concept to scaled adoption. Strong understanding of ethical AI considerations.
  • Excellent communication and collaboration skills.
  • Experience in defining product roadmaps and requirements.
  • Familiarity with AI tools and a data-driven approach.
  • Strong grasp of data privacy (GDPR), regulatory frameworks, security, and AI ethics.
  • Expert backlog management, story writing, acceptance testing, and agile delivery at scale (Scrum/Kanban).
  • Excellent communication and facilitation, able to influence executive, technical, and nontechnical audiences.
  • Technical fluency and eagerness for continuous learning in Data & AI capabilities and products.

What do you offer:

  • Ownership mindset with high accountability for user satisfaction and product reliability.
  • • Pragmatic product instincts: you simplify, focus, and drive value creation and delivery of AI products
  • • Learning agility and curiosity about emerging capabilities and responsible ways to apply them.

What do we offer:

  • A chance to drive innovation by delivering meaningful AI solutions across the EMEA region.
  • A collaborative, global network and supportive coaching culture focused on your growth.
  • Opportunities to lead high
Show more

משרות נוספות שיכולות לעניין אותך

04.09.2025
BS

Boston Scientific Field Clinical Specialist CRM m/w/d Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
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....
תיאור:
#BOSTON SCIENTIFIC
Boston Scientific verändert das Leben durch innovative medizinische Lösungen. Dabei stehen wir an der Spitze der Medizintechnikbranche und entwickeln sie stetig weiter. Bei Boston Scientific geben wir Dir die Möglichkeit, alles was in Dir steckt, einzubringen, indem Du in vielfältigen und leistungsstarken Teams arbeitest und einige der wichtigsten Herausforderungen in der Gesundheitsbranche angehst. Dabei fördern wir Deine Fähigkeiten und Deine Karriere.
Starte Deine Karriere bei Boston Scientific in unserem Team Cardiac Rhythm Management - Herzschrittmacher und Defibrillatoren - für den Großraum München zum nächstmöglichen Zeitpunkt als
Field Clinical Specialist (m/w/d)

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
DEINE VORTEILE
  • 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
Unsere Werte: Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
Wenn Du Lust auf eine neue Herausforderung hast und ein wertvolles Teammitglied von Boston Scientific werden möchtest, dann bewirb Dich mit Deinen vollständigen Bewerbungsunterlagen unter Angabe Deiner Kündigungsfrist und Gehaltsvorstellung.
Wir freuen uns auf Dich!
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, Du fühlst Dich angesprochen.
#LI-Remote
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משרות נוספות שיכולות לעניין אותך

19.07.2025
BS

Boston Scientific Field Clinical Specialist Elektrophysiologie m/w/d Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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.

Show more

משרות נוספות שיכולות לעניין אותך

19.07.2025
BS

Boston Scientific Senior Clinical Evaluation Scientist Germany, North Rhine-Westphalia, Dusseldorf

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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

Show more

משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
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...
תיאור:

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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בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Senior Clinical Evaluation Scientist בחברת Boston Scientific ב-Germany, Dusseldorf. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.