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1.836 results for Clinical Support jobs in East Germany within a 30 km radius
No match yet? There are 1836 more jobs that could match your search
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Biomedical Engineer (m/f/d) at the Else Kröner Fresenius Center for Digital Health
Biomedical Engineer (m/f/d) at the Else Kröner Fresenius Center for Digital Health
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Experience in interdisciplinary collaboration, ideally in a clinical environment, and a strong solution-oriented working style * Mobility: Job bike leasing and subsidy for a public transport ticket to support environmentally friendly commuting * Employee benefits: Staff discounts at our hospital pharmacy, exclusive corporate benefits, and additional shopping portals * Work–life balance: Our Family Office supports you with childcare placements, holiday programs, and caregiving responsibilities.
Experience in interdisciplinary collaboration, ideally in a clinical environment, and a strong solution-oriented working style * Mobility: Job bike leasing and subsidy for a public transport ticket to support environmentally friendly commuting * Employee benefits: Staff discounts at our hospital pharmacy, exclusive corporate benefits, and additional shopping portals * Work–life balance: Our Family Office supports you with childcare placements, holiday programs, and caregiving responsibilities.
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Account Manager TMTT - Hannover/ Magdeburg
Account Manager TMTT - Hannover/ Magdeburg
Edwards Lifesciences GmbH
Hannover, Magdeburg
Partially remote
Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).
Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. To achieve this, we offer on-the-job development, training opportunities and the support and guidance provided by dedicated employee groups (the Edwards Network of Women, Edwards Foundation charity team, sustainability activities, and others).
PhD Position (m/f/d) - Computational Biology & Single-Cell Genomics - Decoding Brain Development
PhD Position (m/f/d) - Computational Biology & Single-Cell Genomics - Decoding Brain Development
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Active contribution to scientific publications and support in project and third-party funding applications with the aim of completing a doctorate (Ph.D. / Dr. rer. * Supervision and technical support of (Bachelor's, Master's, medical students) in daily laboratory and project work - at the Institute of Clinical Genetics * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute
Active contribution to scientific publications and support in project and third-party funding applications with the aim of completing a doctorate (Ph.D. / Dr. rer. * Supervision and technical support of (Bachelor's, Master's, medical students) in daily laboratory and project work - at the Institute of Clinical Genetics * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute
Specialist (m/f/d) in Next-Generation Sequencing
Specialist (m/f/d) in Next-Generation Sequencing
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
Establish and further develop an innovative metagenome sequencing platform for clinical diagnostics and hospital hygiene * Collaborate closely with clinical and diagnostic on methodological and regulatory implementation within healthcare settings * Actively shape a pioneering diagnostics platform with direct clinical and scientific impact * Advantageous: Experience in laboratory diagnostics, validation, or clinical method implementation. at the Institute of Clinical Chemistry and Laboratory Medicine * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute
Establish and further develop an innovative metagenome sequencing platform for clinical diagnostics and hospital hygiene * Collaborate closely with clinical and diagnostic on methodological and regulatory implementation within healthcare settings * Actively shape a pioneering diagnostics platform with direct clinical and scientific impact * Advantageous: Experience in laboratory diagnostics, validation, or clinical method implementation. at the Institute of Clinical Chemistry and Laboratory Medicine * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute
PhD Position (m/f/d) in Developmental Neuroscience
PhD Position (m/f/d) in Developmental Neuroscience
Universitätsklinikum Carl Gustav Carus Dresden
Dresden
at the Institute of Clinical Genetics * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute * Work–Life Balance: Our family office supports you with childcare, holiday programs, and care for relatives.
at the Institute of Clinical Genetics * Mobility: Job bike program and subsidy for public transport tickets to support an environmentally friendly and convenient commute * Work–Life Balance: Our family office supports you with childcare, holiday programs, and care for relatives.
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You will work closely with , , and clinical experts, to ensure our products meet stringent regulatory standards and deliver exceptional performance. * Support visualization workflows (Tableau, Looker, Grafana, or Streamlit).
You will work closely with , , and clinical experts, to ensure our products meet stringent regulatory standards and deliver exceptional performance. * Support visualization workflows (Tableau, Looker, Grafana, or Streamlit).
You will work closely with , , and clinical experts, to ensure our products meet stringent regulatory standards and deliver exceptional performance. * Conduct code reviews and provided technical support to .
You will work closely with , , and clinical experts, to ensure our products meet stringent regulatory standards and deliver exceptional performance. * Conduct code reviews and provided technical support to .
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Auszubildende, Studierende, Fachkräfte im kaufm. und gewerblichen Bereich
Auszubildende, Studierende, Fachkräfte im kaufm. und gewerblichen Bereich
MKT Gebrüder Eschbach GmbH
Ohrdruf
As an Anaesthetic Nurse, you will play a crucial role providing care and support to patients undergoing anaesthesia for surgical or medical procedures. It is important to have the ability to fulfil our framework compliance requirements, including DBS, Occupational Health, Clinical References, and an updated CV. Working with us you will receive first class support and advice from our dedicated team and the opportunity to work flexible shifts to suit your lifestyle in the NHS or private sector.
As an Anaesthetic Nurse, you will play a crucial role providing care and support to patients undergoing anaesthesia for surgical or medical procedures. It is important to have the ability to fulfil our framework compliance requirements, including DBS, Occupational Health, Clinical References, and an updated CV. Working with us you will receive first class support and advice from our dedicated team and the opportunity to work flexible shifts to suit your lifestyle in the NHS or private sector.
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Group Regulatory Affairs Specialist Class II (m/f/d)
Group Regulatory Affairs Specialist Class II (m/f/d)
ONTEX Hygieneartikel Deutschland GmbH
Großpostwitz/Oberlausitz
Evaluates proposed preclinical, clinical and manufacturing documents for regulatory filing and offered plans/strategies (if appropriate) for changes that do not require submissions. * Advises of regulatory requirements for quality, preclinical and clinical data to meet applicable regulations. * May identify, monitor, and submit relevant reports (e.g., Serious Adverse Events) or notifications (e.g., changes in manufacturing) to regulatory authorities during the clinical research process. * Provides regulatory input and support and, as necessary, follow-up for inspections and audits. * Tracks and assesses the scientific and clinical advances that impact healthcare product development and regulations. * Participates in targeted education, clinical science, and evolving science study to meet regulatory requirements for emerging technologies.
Evaluates proposed preclinical, clinical and manufacturing documents for regulatory filing and offered plans/strategies (if appropriate) for changes that do not require submissions. * Advises of regulatory requirements for quality, preclinical and clinical data to meet applicable regulations. * May identify, monitor, and submit relevant reports (e.g., Serious Adverse Events) or notifications (e.g., changes in manufacturing) to regulatory authorities during the clinical research process. * Provides regulatory input and support and, as necessary, follow-up for inspections and audits. * Tracks and assesses the scientific and clinical advances that impact healthcare product development and regulations. * Participates in targeted education, clinical science, and evolving science study to meet regulatory requirements for emerging technologies.
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As part of our expansion into (peri)menopause support, we're looking for a compassionate, proactive, and experienced Menopause Care Expert to guide members and strengthen our internal expertise. As a Menopause Care Expert, you will provide high-quality virtual support to members navigating the menopause transition while serving as a trusted internal expert for our Member Experience team. * Review, audit, and support the development of menopause care content * Help train and support our , sharing knowledge and best practices * Proven experience in menopause care (e.g. menopause nurse, menopause coach, or comparable clinical background) * Mental Health Support: 1:1 psychologist sessions and wellness tools via Nilo Health.
As part of our expansion into (peri)menopause support, we're looking for a compassionate, proactive, and experienced Menopause Care Expert to guide members and strengthen our internal expertise. As a Menopause Care Expert, you will provide high-quality virtual support to members navigating the menopause transition while serving as a trusted internal expert for our Member Experience team. * Review, audit, and support the development of menopause care content * Help train and support our , sharing knowledge and best practices * Proven experience in menopause care (e.g. menopause nurse, menopause coach, or comparable clinical background) * Mental Health Support: 1:1 psychologist sessions and wellness tools via Nilo Health.
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Easy Apply
Partnering with cross-functional teams to support strategic initiatives with data-driven insights. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster.
Partnering with cross-functional teams to support strategic initiatives with data-driven insights. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster.
Easy Apply
We're looking for a creative and detail-oriented Working Student to join our team and support our bilingual content and social media activities. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster.
We're looking for a creative and detail-oriented Working Student to join our team and support our bilingual content and social media activities. * Impact healthcare by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster.
Auszubildende, Studierende, Fachkräfte im kaufm. und gewerblichen Bereich (m/w/d)
Auszubildende, Studierende, Fachkräfte im kaufm. und gewerblichen Bereich (m/w/d)
MKT Gebrüder Eschbach GmbH
Ohrdruf
It is important to have the ability to fulfil our framework compliance requirements, including DBS, Occupational Health, Clinical References, and an updated CV. Working with us you will receive first class support and advice from our dedicated team and the opportunity to work flexible shifts to suit your lifestyle in the NHS or private sector.
It is important to have the ability to fulfil our framework compliance requirements, including DBS, Occupational Health, Clinical References, and an updated CV. Working with us you will receive first class support and advice from our dedicated team and the opportunity to work flexible shifts to suit your lifestyle in the NHS or private sector.
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Support Upstream / Marketing for Value Proposition, Pricing, Product Positioning and Mid-term Portfolio Strategy * Perform product validation in a laboratory and clinical setting * Clinical indication and application knowledge in MIS * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability
Support Upstream / Marketing for Value Proposition, Pricing, Product Positioning and Mid-term Portfolio Strategy * Perform product validation in a laboratory and clinical setting * Clinical indication and application knowledge in MIS * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability
This position serves as a point of contact for medical/clinical issues and is responsible for vigilance as well as Post-Market surveillance and Post-Market Clinical Follow-Up activities, focusing on the evaluation of vigilance data, reporting adverse events and performing recalls/FSCAs and/or corrective actions. * Support with risk analysis and assessment of benefit-risk-ratio
This position serves as a point of contact for medical/clinical issues and is responsible for vigilance as well as Post-Market surveillance and Post-Market Clinical Follow-Up activities, focusing on the evaluation of vigilance data, reporting adverse events and performing recalls/FSCAs and/or corrective actions. * Support with risk analysis and assessment of benefit-risk-ratio
Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc. * Support of audits (customers/authorities and suppliers of medical devices) in coordination and cooperation with the QMR
Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc. * Support of audits (customers/authorities and suppliers of medical devices) in coordination and cooperation with the QMR
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Easy Apply
Our key offerings in the Consumer Healthcare market are: providing strategic innovation consulting covering all aspects of regulatory requirements, science and product development as well as conducting clinical studies (nationally and internationally) for the respective products. * Support of clients in strategic innovation and product development
Our key offerings in the Consumer Healthcare market are: providing strategic innovation consulting covering all aspects of regulatory requirements, science and product development as well as conducting clinical studies (nationally and internationally) for the respective products. * Support of clients in strategic innovation and product development
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Join a team where you can be heard, be supported, and always be yourself. Look again and youâll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. You will be a part of the Field Applications Specialist Team and report to the responsible for providing frontline support by resolving customer(s) problems and issues through technical, scientific expertise and troubleshooting. This is supported with a clear Development Pathway program as part our culture to develop and grow our teams. ⢠Be supported by a strong leadership team, involved in keys projects to deliver successful installations for our Customers that meet their requirements and that of our company. ⢠Provide excellent professional support and training to Beckman Coulterâs customers.
Join a team where you can be heard, be supported, and always be yourself. Look again and youâll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. You will be a part of the Field Applications Specialist Team and report to the responsible for providing frontline support by resolving customer(s) problems and issues through technical, scientific expertise and troubleshooting. This is supported with a clear Development Pathway program as part our culture to develop and grow our teams. ⢠Be supported by a strong leadership team, involved in keys projects to deliver successful installations for our Customers that meet their requirements and that of our company. ⢠Provide excellent professional support and training to Beckman Coulterâs customers.
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Support Upstream / Marketing for Value Proposition, Pricing, Product Positioning and Mid-term Portfolio Strategy * Perform product validation in a laboratory and clinical setting * Clinical indication and application knowledge in MIS * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability
Support Upstream / Marketing for Value Proposition, Pricing, Product Positioning and Mid-term Portfolio Strategy * Perform product validation in a laboratory and clinical setting * Clinical indication and application knowledge in MIS * Contribution and support of risk management process * Coordination of sustaining activities and PM-related Regulatory Processes as Clinical Evaluation, Post Market Surveillance, Post Market Clinical Follow-up, Usability
Collaboration with Regulatory Affairs, Product Management, R&D, and/or external service providers to support PMS, PMCF, Clinical Evaluation documentation - The Medical Affairs (Clinical Affairs) Manager is held responsible for keeping a product or product group compliant with regulations and guidelines. The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products)
Collaboration with Regulatory Affairs, Product Management, R&D, and/or external service providers to support PMS, PMCF, Clinical Evaluation documentation - The Medical Affairs (Clinical Affairs) Manager is held responsible for keeping a product or product group compliant with regulations and guidelines. The employee ensures the proper implementation of procedures that demonstrate the conformity of medical devices with the relevant clinical performance and safety requirements as well as the documentation required by MDR/MEDDEV. * Provide and update regulatory documentation, such as Post Market Surveillance (PMS) Plans, PMS Reports and/or Periodic Safety Update Reports (PSUR), Post-Market Clinical Follow-up (PMCF) documentation (Plan and Report), and/or Clinical Evaluations (Plan and Report) for a product or product group (products in development and new and legacy products)
Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc. * Support of audits (customers/authorities and suppliers of medical devices) in coordination and cooperation with the QMR
Support the development and updating of the design control processes, and of the parallel applicable processes and guidelines * Subject-specific involvement in the implementation of the risk management process, clinical evaluation, and usability file * Control and sole responsibility for reviewing/releasing approval-relevant documents as part of the design control process, in particular Risk analysis/risk management, clinical evaluation, design validation/design verification plans and protocols, software documentation, instructions for use and product labeling * Subject Mater Expert for the interpretation of standard requirements, e.g. for clinical evaluation, biocompatibility, electrical safety, cyber security etc. * Support of audits (customers/authorities and suppliers of medical devices) in coordination and cooperation with the QMR
This position serves as a point of contact for medical/clinical issues and is responsible for vigilance as well as Post-Market surveillance and Post-Market Clinical Follow-Up activities, focusing on the evaluation of vigilance data, reporting adverse events and performing recalls/FSCAs and/or corrective actions. * Support with risk analysis and assessment of benefit-risk-ratio
This position serves as a point of contact for medical/clinical issues and is responsible for vigilance as well as Post-Market surveillance and Post-Market Clinical Follow-Up activities, focusing on the evaluation of vigilance data, reporting adverse events and performing recalls/FSCAs and/or corrective actions. * Support with risk analysis and assessment of benefit-risk-ratio
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Business Support Manager im Kundenservice (m/w/d)
Business Support Manager im Kundenservice (m/w/d)
Lloyds Bank – Bank of Scotland
Berlin
Partially remote
No cover letter required
Easy Apply
Supports the department in its quality assurance initiatives. * Supports the department during internal and external audits. * Supports the in all Data Ownership activities and in the ECB Readiness initiative.
Supports the department in its quality assurance initiatives. * Supports the department during internal and external audits. * Supports the in all Data Ownership activities and in the ECB Readiness initiative.
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You provide IT support to tackle exciting life science problems. * The IT-support will be hosted in the Department of Microbiome Dynamics (MBD) of Prof. Dr. Gianni Panagiotou of the Leibniz-HKI in an international, dynamic team with access to state-of-the-art computational resources.
You provide IT support to tackle exciting life science problems. * The IT-support will be hosted in the Department of Microbiome Dynamics (MBD) of Prof. Dr. Gianni Panagiotou of the Leibniz-HKI in an international, dynamic team with access to state-of-the-art computational resources.
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Senior Support Consultant SAP EWM (m/w/d)
Senior Support Consultant SAP EWM (m/w/d)
Körber Supply Chain Consulting GmbH
Stuttgart, Bad Nauheim, Schwandorf, Dresden, Köln, Heidelberg
Partially remote
Als Senior Support Consultant SAP EWM bist du maßgeblich verantwortlich für einen reibungslosen Ablauf in der Logistik unserer Kunden – von der Störungslösung bis zur Prozessoptimierung. * Betreuung von Bestandskunden: Du unterstützt unsere Kunden im 2nd- und 3rd-Level-Support * Übernahme von Kundensystemen in den Support Regelbetrieb: Du sorgst für eine Übergabe unserer Projekte nach dem GoLive in das Supportteam und stellst den notwendigen Know-how Aufbau im Support-Team sicher. * Weiterentwicklung des Teams: Du unterstützt bei der fachlichen Weiterentwicklung unserer Junior Support Consultants, die von deiner Erfahrung profitieren. * Du bringst Erfahrung im Bereich SAP Beratung (Inhouse oder Extern) oder aus dem SAP EWM Support mit.
Als Senior Support Consultant SAP EWM bist du maßgeblich verantwortlich für einen reibungslosen Ablauf in der Logistik unserer Kunden – von der Störungslösung bis zur Prozessoptimierung. * Betreuung von Bestandskunden: Du unterstützt unsere Kunden im 2nd- und 3rd-Level-Support * Übernahme von Kundensystemen in den Support Regelbetrieb: Du sorgst für eine Übergabe unserer Projekte nach dem GoLive in das Supportteam und stellst den notwendigen Know-how Aufbau im Support-Team sicher. * Weiterentwicklung des Teams: Du unterstützt bei der fachlichen Weiterentwicklung unserer Junior Support Consultants, die von deiner Erfahrung profitieren. * Du bringst Erfahrung im Bereich SAP Beratung (Inhouse oder Extern) oder aus dem SAP EWM Support mit.
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