Gehaltsübersicht für Clinical Research Scientist in Schweiz

The perfect candidate is someone with solid experience in global study management (on a leading level), ideally with experience of early phases, someone with effective leadership skills still able and happy to do operational work. The CRSL is accountable for the strategic and tactical study activities, ensuring high quality execution standards within the agreed budget and timelines Tasks & Responsibilities:Leads the cross-functional Study Management Team (SMT). In the SMT Leader (SMTL) role, the CRSL is responsible for the planning, coordination, communication, motivation and setting the direction of the SMT, including obtaining agreement on study required timelines, budgets, objectives and goal-setting. The SMTL is accountable for the delivery of the clinical studies within the agreed timelines, budget and quality.Prepares and manages the budget/financial plan including overall study and site-level costs, collaborating with the respective stakeholders in contract negotiations and preparation, payment schedule and tracking.Identifies key milestones and tracks critical study activities, issues and strategic priorities. Provides regular updates as appropriate, to key stakeholders.Accountable for all aspects of study management including supply management, biosample management, vendor selection and management, site selection, initiation, training, monitoring, essential document management, closedown and archiving in accordance with current Standard Operating Procedures (SOPs) and ICH Good Clinical Practice (GCP) guidelines.For outsourced studies, contributes to CRO selection activities and contract set-up, serves as primary contact with CRO PM and provides oversight of CRO, ensures communication between CRO, other vendors and SMT for the entire study lifecycle.Assures consistency and standards across a study or studies for all investigational sites and in line with project standards.  Must haves:Minimum 5 years in study management with extensive experience in planning, risk mitigation strategies, trial budgets, site selection, clinical supplies management, sample management, conduct and monitoring of clinical studiesMinimum Bachelor (preference on Master) in Life Sciences Experience with global study managementExperience in pharma (preferred) or CRO Effective leadership skills, able to lead cross-functional teams across multiple time zonesExperience working in matrix environment and flat hierarchical team setting Nice to haves: Experience with early phases of clinical trialsNS & Infection & Oncology

Our MissionOur mission is to solve the most important and fundamental challenges in AI and Robotics to enable future generations of intelligent machines that will help us all live better lives.Research Scientists will have proven hands-on research experience with a focus in one or more of these key areas: Cognitive AI, Athletic AI, Organic Hardware Design or Robot Ethics.  If you have a passion for developing technology for robots and use it to advance their capabilities and usefulness, you will want to join us!  ResponsibilitiesResearch focused on advancing robotic systems by developing exciting new ideas and providing solutions to complex problemsCollaborate on publications to be submitted at worldwide conferencesApply yours and others’ research to real world problemsSystem Design using model based and data driven techniquesCreatively apply modern learning algorithms to real-world problemsUse your strong development skills to develop algorithms and improve systemsWorking with fellow researchers and engineers to develop prototypesRequirementsBS, MS or PhD in a robotics-relevant field5+ years of experience in research and developmentGood grasp of a broad set of techniques related to state and world estimation, active control of dynamic systems and planning/cognitive challenges of these types of systemsStrong development skills with at least one programming languageExperience with systems that have complex physical interaction (locomotion & grasping)BonusProven track record of publications in top-tier conferences and journals in Machine Learning, Robotics, or related fields (e.g. CVPR, ICCV, ECCV, TPAMI, IJCV, NIPS, ICLR, ICML, IJRR, RSS, etc.)  We provide equal employment opportunities to all employees and applicants for employment and prohibit discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.Über das Unternehmen:Boston Dynamics AI Institute

Clinical cytogenomic scientist 100% Oncology laboratory Kinderspital Zürich as an employer Kinderspital Zürich is the largest university children's hospital in Switzerland with about 2,500 employees, and is one of the leading centres for paediatric and youth medicine in Europe. Although the hospital may be big, it's the little ones that count: up to 100,000 patients are cared for each year across 47 faculties, where we do everything in our power to ensure their well being. 'Kispi' not only offers cutting-edge devices and the highest quality of care, but also a good sense of interpersonal issues. Alongside its comprehensive range of paediatric medicine and surgery facilities, the children's hospital also offers a unique rehabilitation centre and a research centre. Your responsibilities Analysis, checking and report of G-banded chromosomes, FISH, miyroarray (CytoScan HD and OncoScan) Somatic NGS and PCR-MRD (can be learned on the job) Performance of external quality assessments Your profile Education as scientists or physicians with many years of experience in cytogenomics Experience in somatic NGS will be of advantage Board certification as clinical cytogeneticist, i.e. FAMH, FachhumangenetikerIn of the GfH, PCCC, ABMG Some knowledge of the German language is advantageous but not mandatory. However, a commitment to learn German should be made Equally patient and motivated to work in an international team PD Dr. Joëlle Tchinda Current Head of the Oncology LaboratoryPhone +41 44 266 70 41 Kinderspital ZürichSteinwiesstrasse 758032 Zürich

StellenbeschreibungGleichen Sie hier die Stellenbeschreibung mit Ihren Job-Präferenzen ab. Sie können die Job-Präferenzen jederzeit in Ihrem Profil verwalten.AnstellungsartTeilzeitArbeitsort4056 Basel, BSBereich Station C, Onkologie/Hämatologie Eintrittsdatum 01.03.2024 Abteilung Das Universitätskinderspital beider Basel (UKBB) ist ein führendes Zentrum der schweizerischen universitären Kindermedizin. Seine Abteilung für pädiatrische Hämatologie und Onkologie betreut jährlich ca. 35 neue KrebspatientInnen im Rahmen von internationalen klinischen Studien und ist eines der 5 universitären Zentren der SPOG. Schwerpunkte der Abteilung sind die Neuroonkologie, die Sarkome und die allogene Stammzelltransplantation. Die Abteilung für pädiatrische Hämatologie und Onkologie sucht eine/-n Clinical Research Coordinator (CRC) (Studiendokumentar/in) 70% Der Einsatz erfolgt im Rahmen des Forschungsverbunds SPOG (Swiss Pediatric Oncology Group). Die SPOG ist der nationale Verein zur Durchführung klinischer Studien für onkologisch / hämatologisch erkrankte Kinder in der Schweiz. Dadurch sollen alle an Krebs erkrankten Kinder und Jugendlichen Zugang zu passenden Behandlungsoptionen kommen. Werden Sie Teil dieses Netzwerks! Hauptaufgaben Koordinative Aufgaben im Rahmen des Forschungsverbunds SPOG für das UKBB Unterstützung der Prüfärztinnen und -ärzte bei der Durchführung von klinischen Studien und wissenschaftlichen Projekten Organisation und Durchführung von Visiten der Studienpatienten/Innen Vorbereitung und Organisation von Studien spezifischen Materialien und Proben einschließlich derer Versand Assistenz bei Protokoll-/ GCP-konformer Durchführung von Studien Erfassung und Meldung von AEs, SAEs und SUSARs Erhebung und Dokumentation von Therapieverläufen und Follow-up’s in CRFs mittels diverser Datenbanken sowie Aktualisierung und Archivierung von Studiendokumenten Vorbereitung und Begleitung von Monitoring-Visiten, Audits und Inspektionen Anforderungen Abgeschlossene Ausbildung als Clinical Research Coordinator (CAS) oder als Pflegefachperson/Study Nurse oder Abschluss in einem medizinischen Assistenzberuf Erfahrung in der Durchführung und Organisation von klinischen Studien nach ICH-GCP von Vorteil Forschungserfahrung in einem Team von Studienkoordinatorinnen und -koordinatoren von Vorteil Begeisterung für die Thematik Ein hohes Maß an Qualitätsbewusstsein, Organisationsfähigkeit sowie eine selbständige und strukturierte Arbeitsweise Sehr gute Team- und Kommunikationsfähigkeit fundierte Computerkenntnisse der gängigen MS-Office Anwendungen und Datenbankprogramme Kenntnisse der med. Terminologie Gute Deutsch- und Englischkenntnisse in Wort und Schrift Wir bieten Eine innovative, interessante und abwechslungsreiche Tätigkeit in einem kleinen, freundlichen und hoch motivierten interdisziplinären Team Regionale und überregionale Zusammenarbeit und Austausch mit KollegInnen Gute Weiterbildungsmöglichkeiten in unserem Netzwerk (SPOG) und an der CTU der Universität Basel Gute Berufsaussichten in einer zukunftssicheren Branche Bewerbungsfrist: 29. Februar 2024 Richten Sie Ihre Bewerbung bitte an: Universitätskinderspital beider Basel UKBB Abteilung für Pädiatrische Hämatologie/Onkologie Prof. Dr. med. Nicolas von der Weid, Abteilungsleiter Spitalstrasse 33 4031 Basel E-Mail: [email protected] Erstellen Sie ein Indeed-Konto, bevor Sie zur Website des Unternehmens weitergeleitet werden.

Die Abteilung für pädiatrische Hämatologie und Onkologie sucht eine/-nClinical Research Coordinator (CRC) (Studiendokumentar/in) 70%Der Einsatz erfolgt im Rahmen des Forschungsverbunds SPOG (Swiss Pediatric Oncology Group). Die SPOG ist der nationale Verein zur Durchführung klinischer Studien für onkologisch / hämatologisch erkrankte Kinder in der Schweiz. Dadurch sollen alle an Krebs erkrankten Kinder und Jugendlichen Zugang zu passenden Behandlungsoptionen kommen. Werden Sie Teil dieses Netzwerks!Hauptaufgaben:Koordinative Aufgaben im Rahmen des Forschungsverbunds SPOG für das UKBB Unterstützung der Prüfärztinnen und -ärzte bei der Durchführung von klinischen Studien und wissenschaftlichen Projekten Organisation und Durchführung von Visiten der Studienpatienten/Innen Vorbereitung und Organisation von Studien spezifischen Materialien und Proben einschließlich derer Versand Assistenz bei Protokoll-/ GCP-konformer Durchführung von Studien Erfassung und Meldung von AEs, SAEs und SUSARs Erhebung und Dokumentation von Therapieverläufen und Follow-up's in CRFs mittels diverser Datenbanken sowie Aktualisierung und Archivierung von Studiendokumenten Vorbereitung und Begleitung von Monitoring-Visiten, Audits und Inspektionen Anforderungen:Abgeschlossene Ausbildung als Clinical Research Coordinator (CAS) oder als Pflegefachperson/Study Nurse oder Abschluss in einem medizinischen Assistenzberuf Erfahrung in der Durchführung und Organisation von klinischen Studien nach ICH-GCP von Vorteil Forschungserfahrung in einem Team von Studienkoordinatorinnen und -koordinatoren von Vorteil Begeisterung für die Thematik Ein hohes Maß an Qualitätsbewusstsein, Organisationsfähigkeit sowie eine selbständige und strukturierte Arbeitsweise Sehr gute Team- und Kommunikationsfähigkeit fundierte Computerkenntnisse der gängigen MS-Office Anwendungen und Datenbankprogramme Kenntnisse der med. Terminologie Gute Deutsch- und Englischkenntnisse in Wort und Schrift Wir bieten:Eine innovative, interessante und abwechslungsreiche Tätigkeit in einem kleinen, freundlichen und hoch motivierten interdisziplinären Team Regionale und überregionale Zusammenarbeit und Austausch mit KollegInnen Gute Weiterbildungsmöglichkeiten in unserem Netzwerk (SPOG) und an der CTU der Universität Basel Gute Berufsaussichten in einer zukunftssicheren Branche Bewerbungsfrist: 29. Februar 2024Richten Sie Ihre Bewerbung bitte an:Universitätskinderspital beider Basel UKBBAbteilung für Pädiatrische Hämatologie/Onkologie Prof. Dr. med. Nicolas von der Weid, AbteilungsleiterSpitalstrasse 334031 BaselE-Mail: [email protected] freuen uns auf Ihre Online-Bewerbung!Bitte nehmen Sie sich einen kurzen Moment Zeit und füllen Sie die Felder auf der nächsten Seite aus. Halten Sie dazu Ihre vollständigen Bewerbungsunterlagen elektronisch bereit.Bei allgemeinen Fragen zur Stelle oder zum Bewerbungsprozess hilft Ihnen unser HR Team, Telefon +41 61 704 12 32 gerne weiter.Wir freuen uns auf Ihre Online-Bewerbung!Bitte nehmen Sie sich einen kurzen Moment Zeit und füllen Sie die Felder auf der nächsten Seite aus. Halten Sie dazu Ihre vollständigen Bewerbungsunterlagen elektronisch bereit.Bei allgemeinen Fragen zur Stelle oder zum Bewerbungsprozess hilft Ihnen unser HR Team, Telefon +41 61 704 12 32 gerne weiter.Universitäts-Kinderspital beider Basel Basel Unbefristet Vollzeit 5 Stunden her Bereich:Station C, Onkologie/HämatologieEintrittsdatum:01.03.2024Abteilung:Das Universitätskinderspital beider Basel (UKBB) ist ein führendes Zentrum der schweizerischen universitären Kindermedizin. Seine Abteilung für pädiatrische Hämatologie und Onkologie betreut jährlich ca. 35 neue KrebspatientInnen im Rahmen von internationalen klinischen Studien und ist eines der 5 universitären Zentren der SPOG. Schwerpunkte der Abteilung sind die Neuroonkologie, die Sarkome und die allogene Stammzelltransplantation.

Our Company Changing the world through digital experiences is what Adobe’s all about. We give everyone—from emerging artists to global brands—everything they need to design and deliver exceptional digital experiences! We’re passionate about empowering people to create beautiful and powerful images, videos, and apps, and transform how companies interact with customers across every screen. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We realize that new ideas can come from everywhere in the organization, and we know the next big idea could be yours! Job Description Our Company Changing the world through digital experiences is what Adobe’s all about. We give everyone—from emerging artists to global brands—everything they need to design and deliver exceptional digital experiences. We’re passionate about empowering people to craft beautiful and powerful images, videos, and apps, and transform how companies interact with customers across every screen. We’re on a mission to hire the very best and are committed to building exceptional employee experiences where everyone is respected and has access to equal opportunity. We realize that new ideas can come from everywhere in the organization, and we know the next big idea could be yours. The Role Adobe Research is seeking a research scientist who is a newly Ph.D. graduate specializing in the development of innovative software and hardware systems for human-computer interaction (HCI). You will have expertise in computer vision, machine learning, digital fabrication, computational imaging, and related cutting-edge technologies. You will develop novel technologies seamlessly identifying, tracking, and interacting with real-world objects in mixed reality (AR/VR) and ubiquitous computing environments. As a research scientist at Adobe, you will be joining a dynamic team of computer systems, machine learning, and deep learning researchers to build the future of digital experiences. You will have the opportunity to develop creative ideas suitable for academic publication, to mentor interns, and to participate in our university collaboration program. You will also work with product teams to implement those ideas as advanced features in Adobe's world-class products, thereby reaching millions of people worldwide. What you'll do • Provide technical and design leadership across multiple teams, leveraging expertise in human-computer interaction (HCI), digital fabrication, and mixed reality. • Furnish innovations that fuel the growth of Adobe by developing novel technologies and solutions that bridge the gap between the physical and digital realms. • Collaborate with world-class researchers and engineers to bring research ideas from conception to production. • Develop innovative algorithms and approaches that leverage Adobe products in mixed reality environments, enabling the seamless connection between the digital and physical customer journeys, enhancing the understanding of user behavior, and informing the design of immersive experiences. • Document research findings thoroughly and maintain well-organized code to ensure reproducibility and facilitate knowledge transfer within the research team and beyond. • Publish and present work in world-class scientific venues in human-computer interaction (HCI). What you'll need to succeed • Ph.D. in Human-Computer Interaction, Computer Science, or a related field. • Solid programming skills, including mixed reality prototyping (C#, Unity), web development (HTML, CSS, JavaScript), and proficiency in machine learning and image processing frameworks for computer vision and sensing (PyTorch, fastai, OpenCV, Matlab). • Strong skills in hardware development, including digital fabrication (3D printing, laser cutting) and computational sensing and imaging (sensors, cameras). • Strong peer-reviewed publication track record • Desire to do world-class publishable research and develop advanced features for Adobe’s imaging, video, and analytics products Adobe is proud to be an Equal Employment Opportunity and affirmative action employer. We do not discriminate based on gender, race or color, ethnicity or national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status, or any other applicable characteristics protected by law. Learn more. Adobe aims to make Adobe.com accessible to any and all users. If you have a disability or special need that requires accommodation to navigate our website or complete the application process, email [email protected] or call (408) 536-3015. Adobe values a free and open marketplace for all employees and has policies in place to ensure that we do not enter into illegal agreements with other companies to not recruit or hire each other’s employees. At Adobe, you will be immersed in an exceptional work environment that is recognized around the world. You will also be surrounded by colleagues who are committed to helping each other grow through our unique Check-In approach where ongoing feedback flows freely. If you’re looking to make an impact, Adobe's the place for you. Discover what our employees are saying about their career experiences on the Adobe Life blog and explore the meaningful benefits we offer. There's more than meets the eye when it comes to Adobe. Take the quiz and see how well you know us! Adobe is proud to be an Equal Employment Opportunity and affirmative action employer. We do not discriminate based on gender, race or color, ethnicity or national origin, age, disability, religion, sexual orientation, gender identity or expression, veteran status, or any other applicable characteristics protected by law. Learn more. Adobe aims to make Adobe.com accessible to any and all users. If you have a disability or special need that requires accommodation to navigate our website or complete the application process, email [email protected] or call (408) 536-3015. Adobe values a free and open marketplace for all employees and has policies in place to ensure that we do not enter into illegal agreements with other companies to not recruit or hire each other’s employees.Über das Unternehmen:DMCH-Adobe Research (Schweiz) AG

Die Universitätsklinik für Kardiologie ist Teil des Schweizer Herz- und Gefässzentrums Bern am Inselspital. Die „MedizinischeForschung“ der Universitätsklinik für Kardiologie ist mitverantwortlich für die Planung und Durchführung von klinischen Studien. Sie ist die Schnittstelle zwischen Patienten, Prüfärzten und Monitoren der pharmazeutischen und medizintechnischen Industrie sowie der Universitätsklinik. Die Tätigkeiten erfolgen auf der Grundlage der Guten Klinischen Praxis (GCP) sowie dem schweizerischen Humanforschungsgesetz (HFG). Das erwartet SieSie unterstützen die Prüfärzte bei der prüfplangerechten Durchführung von klinischen Studien, teils in Zusammenarbeit mit externen Partnern. Dazu gehören die Koordination und Durchführung von komplexen Studien, Planung und Durchführung von Patientenvisiten sowie Pflege der Studienordner. Das bringen Sie mitNaturwissenschaftliches Studium (Master oder Bachelor)Idealerweise erste Erfahrungen in der Durchführung von klinischen StudienStilsicher in Deutsch, mündliche Französischkenntnisse, gute EnglischkenntnisseGenaue Arbeitsweise und VerantwortungsbewusstseinOrganisationstalentUnser AngebotEine spannende Mitarbeit an innovativen und zukunftsweisenden ForschungsprojektenSämtliche Vorteile eines UniversitätsspitalsUnterstützung durch ein erfahrenes TeamStelleninformationenOrganisation Medizinbereich Herz / GefässPensum 80 - 100 %Eintritt per 01.04.2024 oder n. V.befristet mit Aussicht auf VerlängerungKennziffer 16372Vertragsart befristetArbeitsort Inselspital, Universitätsspital BernFreiburgstrasse, CH-3010 BernSchweizStelleninformationenWiss. Mitarbeiter:in / Clinical Research Manager (w/m/d)Bern, 80 - 100 %

Senior Research Scientist Distributed Computer SystemsSenior Research Scientist Distributed Computer Systems Ref. 2023_026 IBM Research Europe – Zurich is one of IBM’s 12 global research labs. Our mission comprises cutting-edge research for tomorrow’s information technology and inventing what’s next in computing. Our activities include applied research in the areas of Hybrid Cloud, AI, Security, and Quantum computing as well as fundamental science research. We cultivate close relationships with academic and industrial partners and are part of the local and global scientific community to help drive Europe’s innovation agenda. We are seeking an outstanding and passionate Senior Research Scientist to join our team. You will play an essential role in developing bleeding-edge cloud-first storage solutions and supporting our research teams in a highly collaborative and international research environment. If you're excited about driving groundbreaking systems work, solving complex problems, and supporting other team members, we want to hear from you. Your responsibilities will include: Being the technical lead of a team building and enhancing IBM products and technologies. Mentoring both researchers and software developers, offering guidance and experienced thinking. Collaborating with external industry and academic partners and applying for external funding. The minimum requirements for this role are as follows: Ph.D. in computer science coupled with a strong publication record in a relevant systems area. At least 5 years of professional experience after graduation. Experience leading either research or development teams. To excel in this role, the following qualifications are desired: Hands-on experience with distributed storage systems (e.g., Ceph, Spectrum Scale). Deep understanding of the modern IO stack (e.g., io_uring/SPDK, CXL, ZNS/FDB storage extensions). Knowledge of modern non-volatile media technologies and the internals of NVMe SSDs. Experience with cloud virtualization technologies such as the Kubernetes or OpenShift platforms. Strong teamwork skills and a desire to contribute and help proactively. Diversity IBM is committed to diversity at the workplace. With us you will find an open, multicultural environment. Excellent flexible working arrangements enable all genders to strike the desired balance between their professional development and their personal lives. How to apply If you are excited to be a part of IBM Research's mission to shape the future of technology, please submit your CV and motivation reasons. Apply For technical questions, please contact Dr. Radu Stoica, Manager Infrastructure Software at [email protected].

Clinical Research FellowshipThe EOC the multisite hospital of Ticino is present with its institutions on the entire cantonal territory with a total of 1,000 beds. The organization makes it possible to effectively combine local approach and overall vision, guaranteeing the population a comprehensive and proximity hospital offer, regardless of where services are required.Thanks to the commitment and expertise of its more than 5,000 employees and their focus on human relationships, the EOC ensures quality health care for 380,000 patients a year. To complete the team at the Oncological Institute of Southern Switzerland (IOSI) Bellinzona, New Drugs Development Unit, we are looking for a/an Clinical Research Fellowship (100%) The Oncology Institute of Southern Switzerland is one of the largest clinical research centers in Switzerland. Our three main areas of clinical research comprise new drug development, lymphoproliferative diseases (lymphoma and chronic lymphocytic leukaemia) and prostate cancer. Other important areas of development in clinical research include gynecological cancer, breast, lung, skin and gastrointestinal cancer.The IOSI has a dedicated phase 1 unit where early phase clinical trials, including first-in-human, are conducted. We have an excellent history of collaborating with both non-for-profit academic organizations and the pharmaceutical industry. Of particular relevance are our collaborations with the Institute of Oncology Research (IOR), the Institute of Biochemical Research (IRB) and the Swiss Group for Clinical Cancer Research (SAKK). We have a central role in the Faculty of Biomedical Sciences of the Università della Svizzera Italiana (USI). We are offering a Clinical Research fellowship in Drug Development in solid tumors. This fellowship would incorporate activities in the phase 1 Unit of the IOSI and clinical activity. During the fellowship program, there will be the possibility to participate in educational activities performed in our institute and selected external events. Through this fellowship, you will develop your clinical skills, increase your knowledge on how to conduct clinical research and manage patients enrolled in clinical trials, particularly focusing on early phase clinical trials. A minimum commitment of one year is required, to allow you to complete the fellowship objectives. Job Summary/Objectives: Develop clinical expertise in the management of patients with solid tumors enrolled in early phase clinical trials Learn the different aspects of the clinical research, particularly regarding trial design, evaluation of treatment toxicity and efficacy, management of patients enrolled in clinical trials, with a focus on early phase clinical trials of novel therapeutics Participation in study-specific safety calls in collaboration with the principal investigator and the Clinical Research Unit (CRU) team Attend internal meetings and educational activities Partecipate in multidisciplinary tumour boards Partecipations in research projects with clinical or translational objectives Conceptualize and conduct at least one specific research project that is realizable within the period of the fellowship Publish manuscripts in peer-reviewed journals Salary: The per annum rate is approximately 40’000 CHF, the Swiss mandatory health insurancecosts will be deducted from this before payment to the post holder. Candidates receiving agrant from their institution or from a national or international society, will instead have theirgrant topped up to this level. Travel and accommodation costs are considered as includedin this salary and there will be no additional payments made. Eligibility Candidates must be/have:- A medicine degree - Experience in medical oncology of at least 2 years- Proficient in Italian for patients and clinics, minimum B2 level (if non-native Italian speaker)- Proficient in English, as this is the primary language of research and related communications You should also verify your eligibility for registering with (MEBEKO). However, we recommend you do not apply to register with MEBEKO at this point. For more information you can write to the e-mail adress: [email protected], [email protected] or [email protected]. No paper applications will be accepted. EOC - il nostro ospedale. Interessato? Se si riconosce nel profilo e nei valori ricercati, invii la sua candidatura »Indietro

Clinical cytogenomic scientist 100% Oncology laboratory Kinderspital Zürich as an employer Kinderspital Zürich is the largest university children's hospital in Switzerland with about 2,500 employees, and is one of the leading centres for paediatric and youth medicine in Europe. Although the hospital may be big, it's the little ones that count: up to 100,000 patients are cared for each year across 47 faculties, where we do everything in our power to ensure their well being. 'Kispi' not only offers cutting-edge devices and the highest quality of care, but also a good sense of interpersonal issues. Alongside its comprehensive range of paediatric medicine and surgery facilities, the children's hospital also offers a unique rehabilitation centre and a research centre. Your responsibilities Analysis, checking and report of G-banded chromosomes, FISH, miyroarray (CytoScan HD and OncoScan) Somatic NGS and PCR-MRD (can be learned on the job) Performance of external quality assessments Your profile Education as scientists or physicians with many years of experience in cytogenomics Experience in somatic NGS will be of advantage Board certification as clinical cytogeneticist, i.e. FAMH, FachhumangenetikerIn of the GfH, PCCC, ABMG Some knowledge of the German language is advantageous but not mandatory. However, a commitment to learn German should be made Equally patient and motivated to work in an international team Dr. rer. nat. Birgit Krabichler Oncology LaboratoryPhone +41 44 266 32 79 Kinderspital ZürichSteinwiesstrasse 758032 Zürich