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11 Treffer für Clinical Jobs in Weiterstadt im Umkreis von 30 km
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Clinical Research Associate (CRA) (m/w/d)
Clinical Research Associate (CRA) (m/w/d)
GBG Forschungs GmbH
Neu-Isenburg bei Frankfurt am Main
Teilweise Home-Office
Als Clinical Research Associate (CRA) übernehmen Sie die Verantwortung für die Überwachung und Qualitätssicherung klinischer Studien. Bridging the gap between clinical excellence and operational efficiency.
Als Clinical Research Associate (CRA) übernehmen Sie die Verantwortung für die Überwachung und Qualitätssicherung klinischer Studien. Bridging the gap between clinical excellence and operational efficiency.
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Develop and execute the EMEA KOL strategy: Identify, recruit, and manage , clinical experts, and influential to strengthen the company's educational and marketing impact in the region * Coordinate clinical education and advocacy programs: Plan and manage KOL-led webinars, workshops, speaking engagements, training sessions, and clinical demonstration events across EMEA * Drive clinical content creation: Collaborate with KOLs to produce high-quality case studies, clinical videos, whitepapers, and scientific presentations that highlight the value of dental 3D printing applications * Support product launches with expert voices: Engage KOLs in launch campaigns, pilot programs, and feedback cycles to refine messaging and ensure strong clinical validation * Manage KOL contracts and performance: Oversee agreements, deliverables, budgets, and KPIs for all KOL collaborations to ensure alignment with ...
Develop and execute the EMEA KOL strategy: Identify, recruit, and manage , clinical experts, and influential to strengthen the company's educational and marketing impact in the region * Coordinate clinical education and advocacy programs: Plan and manage KOL-led webinars, workshops, speaking engagements, training sessions, and clinical demonstration events across EMEA * Drive clinical content creation: Collaborate with KOLs to produce high-quality case studies, clinical videos, whitepapers, and scientific presentations that highlight the value of dental 3D printing applications * Support product launches with expert voices: Engage KOLs in launch campaigns, pilot programs, and feedback cycles to refine messaging and ensure strong clinical validation * Manage KOL contracts and performance: Oversee agreements, deliverables, budgets, and KPIs for all KOL collaborations to ensure alignment with ...
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ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development - We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. * Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Performing data review and resolution of queries to maintain high-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development - We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. * Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Performing data review and resolution of queries to maintain high-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports
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Clinical Scientist (m/w/d)
Clinical Scientist (m/w/d)
Grifols Deutschland GmbH
Niederrad, 60 Frankfurt am Main-Frankfurt-Süd, Deutschland
Die Stelle ist dem Clinical Development Team * Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
Die Stelle ist dem Clinical Development Team * Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
Bridging the gap between clinical excellence and operational efficiency.
Bridging the gap between clinical excellence and operational efficiency.
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Lifecare Germany GmbH, part of the Lifecare Group, is a clinical-stage medical sensor company developing advanced technologies for the sensing and monitoring of various body analytes. In addition to R&D, our laboratory provides commercial services for the pharmaceutical and biotechnology industries, supporting clinical research, testing and approval processes for drugs and medical devices, as well as general laboratory services for medical institutions.
Lifecare Germany GmbH, part of the Lifecare Group, is a clinical-stage medical sensor company developing advanced technologies for the sensing and monitoring of various body analytes. In addition to R&D, our laboratory provides commercial services for the pharmaceutical and biotechnology industries, supporting clinical research, testing and approval processes for drugs and medical devices, as well as general laboratory services for medical institutions.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. * Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring ...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Principal Medical Writer to join our diverse and dynamic team. As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical information. * Develop regulatory documents for submission to regulatory agencies globally, including Clinical Study Reports, Clinical Summaries of Efficacy and Safety, and Clinical Overviews, in accordance with ICH and other global guidelines, standards and processes, and Incyte authoring ...
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Challenging work which supports the development of new and better ways to improve clinical outcomes for oncology treatment around the world.
Challenging work which supports the development of new and better ways to improve clinical outcomes for oncology treatment around the world.
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The company is focused on investing in high quality product development efforts, as well as rigorous clinical studies to create a strong foundation for future clinical adoption. This individual will work closely with the Global Market Access team & external consultants, making use of clinical data and economic models, to establish appropriate justifications for reimbursement and coverage. * Foster a close and effective working relationship across all relevant departments and teams, especially sales & marketing, regulatory and clinical/scientific affairs * Facilitate Key Opinion Leader (KOL) and Clinical Society conversations as required * Keep up to date on clinical trials, both investigator initiated and external studies, that can be used to improve clinical and health economic value messaging for Recor Medical products or categories
The company is focused on investing in high quality product development efforts, as well as rigorous clinical studies to create a strong foundation for future clinical adoption. This individual will work closely with the Global Market Access team & external consultants, making use of clinical data and economic models, to establish appropriate justifications for reimbursement and coverage. * Foster a close and effective working relationship across all relevant departments and teams, especially sales & marketing, regulatory and clinical/scientific affairs * Facilitate Key Opinion Leader (KOL) and Clinical Society conversations as required * Keep up to date on clinical trials, both investigator initiated and external studies, that can be used to improve clinical and health economic value messaging for Recor Medical products or categories
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Associate Principal/Principal Medical Writers (F, M or D)
Associate Principal/Principal Medical Writers (F, M or D)
Trilogy Writing & Consulting GmbH
Frankfurt am Main
Our writers are integral members of clinical development teams supporting the writing and coordination of successful documentation across a broad spectrum of therapeutic areas. - Function as a lead writer to prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) in collaboration with members of client authoring teams and supported by other , as appropriate. - Must have worked as the lead writer on several key regulatory documents such as: Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications. - Must have in-depth working knowledge of the relevant regulatory guidance (e.g. ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance.
Our writers are integral members of clinical development teams supporting the writing and coordination of successful documentation across a broad spectrum of therapeutic areas. - Function as a lead writer to prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) in collaboration with members of client authoring teams and supported by other , as appropriate. - Must have worked as the lead writer on several key regulatory documents such as: Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications. - Must have in-depth working knowledge of the relevant regulatory guidance (e.g. ICH, FDA, EMA) for clinical trial conduct, including document-specific guidance.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental ...
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Study Start Up Associate II at ICON, you will play a pivotal role in leading the initiation of clinical trials, ensuring the successful negotiation and on-going maintenance of clinical trial agreements, complex amendments, and other ancillary agreements with study sites. * Drafts, reviews, negotiates, and finalizes clinical trial agreements, complex amendments, and other ancillary agreements with study sites using critical thinking, available tools/systems/documents, historical data, and adheres to departmental and/or client quality check requirements in a manner that protects ICON's fundamental ...
10 passende Jobs liegen außerhalb deiner Region
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Unterstützung des Clinical Supply Teams bei Planung und Ausführung standardisierter Tätigkeiten zur Verpackung und Etikettierung von Prüfpräparaten
Unterstützung des Clinical Supply Teams bei Planung und Ausführung standardisierter Tätigkeiten zur Verpackung und Etikettierung von Prüfpräparaten
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Werkstudent (m/w/d) im Bereich Personal Branding LinkendIn
Werkstudent (m/w/d) im Bereich Personal Branding LinkendIn
Invisio Clinical Studies Consulting GmbH
Mannheim
Teilweise Home-Office
Invisio Clinical Studies Consulting GmbH
Invisio Clinical Studies Consulting GmbH
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(Senior) Manager (m/f/d) Supplier Compliance Management Packaging (Technical Packaging Expert)
(Senior) Manager (m/f/d) Supplier Compliance Management Packaging (Technical Packaging Expert)
Fresenius Kabi Deutschland GmbH
Bad Homburg
We save and improve human lives with affordable, accessible, and innovative healthcare products and the highest quality in clinical care. Fresenius Kabi's product portfolio includes a range of highly complex biopharmaceuticals, clinical nutrition, medical devices and generic intravenous drugs, serving 450 million people annually.
We save and improve human lives with affordable, accessible, and innovative healthcare products and the highest quality in clinical care. Fresenius Kabi's product portfolio includes a range of highly complex biopharmaceuticals, clinical nutrition, medical devices and generic intravenous drugs, serving 450 million people annually.
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Stellvertretende Schulleitung (m/w/d) für die Schule für Pflegeberufe
Stellvertretende Schulleitung (m/w/d) für die Schule für Pflegeberufe
St. Dominikus Krankenhaus und Jugendhilfe gGmbH
Ludwigshafen am Rhein, Deutschland
Moderne technische Ausstattung der Schule mit digitalen Tafeln, Nursing Anneund Clinical Key StudentTM education Plattform
Moderne technische Ausstattung der Schule mit digitalen Tafeln, Nursing Anneund Clinical Key StudentTM education Plattform
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Clinical Support Specialist STIWELL Deutschland (m/w/d)
Clinical Support Specialist STIWELL Deutschland (m/w/d)
MED-EL Medical Electronics
Deutschland, Home Office
als klinische/n Außendienstmitarbeiter*in „Clinical Support Specialist STIWELL Neurorehabilitation“ für Funktionelle Elektrostimulation (FES) in Vollzeit.
als klinische/n Außendienstmitarbeiter*in „Clinical Support Specialist STIWELL Neurorehabilitation“ für Funktionelle Elektrostimulation (FES) in Vollzeit.
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Clinical Sales Director Central Europe (m/w/d)
Clinical Sales Director Central Europe (m/w/d)
BIOMERIEUX
bundesweit, Schweiz, Österreich, Polen, Tschechien, Slowakei, Ungarn, Osteuropa
Teilweise Home-Office
Senior Clinical Sales Director Central Europe * More than 5 years of senior commercial management experience in the clinical diagnostic / healthcare market with a proven track record
Senior Clinical Sales Director Central Europe * More than 5 years of senior commercial management experience in the clinical diagnostic / healthcare market with a proven track record
BIOMERIEUX * bundesweit * Feste Anstellung * Homeoffice möglich, Vollzeit - Als ein weltweit führendes Unternehmen im Bereich der In-vitro-Diagnostik stellt bioMérieux seit über 60 Jahren diagnostische Lösungen bereit, mit denen sich die Quellen von Krankheiten und Kontaminationen ermittlen lassen – für eine bessere Patientenversorgung und mehr Verbrauchersicherheit. Willst Du dazu beitragen, weltweit Leben zu retten? Werde Teil der über 13.000 Mitarbeiterinnen und Mitarbeiter von bioMérieux! Deine Aufgaben - Wir suchen einen Key Account Manager (m/w/d) – Klinischer Bereich - Standort: Remote in Deutschland - Für unsere größten Key Accounts (Verbunds-Kunden) suchen wir einen Key Account Manager in Deutschland, der die Kundenbeziehung in allen Aspekten pflegt und kreativ gestaltet. Du hast Lust, die Welt zu einem gesünderen Ort zu machen? Dann bist Du bei uns genau richtig!
BIOMERIEUX * bundesweit * Feste Anstellung * Homeoffice möglich, Vollzeit - Als ein weltweit führendes Unternehmen im Bereich der In-vitro-Diagnostik stellt bioMérieux seit über 60 Jahren diagnostische Lösungen bereit, mit denen sich die Quellen von Krankheiten und Kontaminationen ermittlen lassen – für eine bessere Patientenversorgung und mehr Verbrauchersicherheit. Willst Du dazu beitragen, weltweit Leben zu retten? Werde Teil der über 13.000 Mitarbeiterinnen und Mitarbeiter von bioMérieux! Deine Aufgaben - Wir suchen einen Key Account Manager (m/w/d) – Klinischer Bereich - Standort: Remote in Deutschland - Für unsere größten Key Accounts (Verbunds-Kunden) suchen wir einen Key Account Manager in Deutschland, der die Kundenbeziehung in allen Aspekten pflegt und kreativ gestaltet. Du hast Lust, die Welt zu einem gesünderen Ort zu machen? Dann bist Du bei uns genau richtig!
The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) * Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) * Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
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Coaching und Sales Excellence: Du entwickelst Clinical-Selling-Kompetenzen, Verhandlungssicherheit und die kommunikative Wirkung deiner Mitarbeitenden gezielt weiter. * Souveräne Clinical-Selling-Kompetenz sowie sichere Zusammenarbeit mit :innen, OP-Teams und wirtschaftlichen Stakeholdern
Coaching und Sales Excellence: Du entwickelst Clinical-Selling-Kompetenzen, Verhandlungssicherheit und die kommunikative Wirkung deiner Mitarbeitenden gezielt weiter. * Souveräne Clinical-Selling-Kompetenz sowie sichere Zusammenarbeit mit :innen, OP-Teams und wirtschaftlichen Stakeholdern
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Senior Manager / Associate Director Corporate Affairs, Germany (Government Affairs and Patient Advocacy)
Senior Manager / Associate Director Corporate Affairs, Germany (Government Affairs and Patient Advocacy)
BeiGene Germany GmbH
Germany Remote
Work closely with internal departments, including Clinical, Regulatory, Medical, Market Access, Legal, and Commercial teams, to align government affairs and patient advocacy strategies with business objectives.
Work closely with internal departments, including Clinical, Regulatory, Medical, Market Access, Legal, and Commercial teams, to align government affairs and patient advocacy strategies with business objectives.
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2-4 years of experience in the pharmaceutical industry (Medical Affairs roles e.g., Medical Manager/Advisor, MSL) with proven expertise in at least one therapeutic area * Lead initiatives to enhance excellence of field medical teams in collaboration with CEX, BTS, and medical training managers * Ensure local Medical Excellence & Operations activities comply with all AbbVie processes, the Code of Business Conduct, ethics, regulatory requirements, and local laws * Proactively contribute to and implement global strategies in close cross-functional collaboration, supporting best-in-class medical infield team excellence * Develop and implement processes, tools, and materials to drive Medical Excellence AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.
2-4 years of experience in the pharmaceutical industry (Medical Affairs roles e.g., Medical Manager/Advisor, MSL) with proven expertise in at least one therapeutic area * Lead initiatives to enhance excellence of field medical teams in collaboration with CEX, BTS, and medical training managers * Ensure local Medical Excellence & Operations activities comply with all AbbVie processes, the Code of Business Conduct, ethics, regulatory requirements, and local laws * Proactively contribute to and implement global strategies in close cross-functional collaboration, supporting best-in-class medical infield team excellence * Develop and implement processes, tools, and materials to drive Medical Excellence AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow.
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Für unseren Standort in Reinheim suchen wir Sie als Specialist (gn) im Qualitätsmanagement. * Merz Pharma GmbH Co. KGaA * Reinheim * Befristeter Vertrag * Vollzeit - Sei einer der ersten Bewerber - Sie haben Interesse daran, Ihr Talent in einem dynamischen Pharma-Unternehmen mit mehr als 115 Jahren Tradition auszuleben? Dann sind Sie bei der Merz Pharma GmbH & Co. KGaA im Geschäftsbereich Merz Toxin Technology & Supply (MTTS) an der richtigen Adresse! Wer wir sind: Mit den drei Geschäftseinheiten Merz Aesthetics, Merz Therapeutics und Merz Lifecare nimmt Merz eine führende Position auf den Märkten der Welt ein. Der Großteil der Produktherstellung und -auslieferung inklusive aller zugehörigen Prozesse liegt bei MTTS. Was uns im gesamten Unternehmen auszeichnet, sind ein ausgeprägter Innovationsgeist, erstklassige Produkte und Services, das Engagement unserer Mitarbeitenden und ein starker Teamspirit.
Für unseren Standort in Reinheim suchen wir Sie als Specialist (gn) im Qualitätsmanagement. * Merz Pharma GmbH Co. KGaA * Reinheim * Befristeter Vertrag * Vollzeit - Sei einer der ersten Bewerber - Sie haben Interesse daran, Ihr Talent in einem dynamischen Pharma-Unternehmen mit mehr als 115 Jahren Tradition auszuleben? Dann sind Sie bei der Merz Pharma GmbH & Co. KGaA im Geschäftsbereich Merz Toxin Technology & Supply (MTTS) an der richtigen Adresse! Wer wir sind: Mit den drei Geschäftseinheiten Merz Aesthetics, Merz Therapeutics und Merz Lifecare nimmt Merz eine führende Position auf den Märkten der Welt ein. Der Großteil der Produktherstellung und -auslieferung inklusive aller zugehörigen Prozesse liegt bei MTTS. Was uns im gesamten Unternehmen auszeichnet, sind ein ausgeprägter Innovationsgeist, erstklassige Produkte und Services, das Engagement unserer Mitarbeitenden und ein starker Teamspirit.
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med publico GmbH * Wiesbaden * Feste Anstellung * Vollzeit - Medizin, Gesundheit, Kommunikation – das ist seit 2007 unsere Leidenschaft. Du brennst für Deine Arbeit mit Kunden und möchtest Dich beruflich verändern? med publico ist eine medizinisch-wissenschaftliche Business Unit der wikonect GmbH. Wir beraten und betreuen führende Unternehmen und Institutionen aus der Pharmazeutischen Industrie und suchen Dich! Zur Verstärkung unseres bestehenden Teams mit mehr als 60 Mitarbeitenden suchen wir zum nächstmöglichen Zeitpunkt eine(n) Vollzeit, unbefristet - am Standort Wiesbaden - Du bist unkonventionell, ideenreich und liebst Deinen Beruf. – Dann bist Du genau richtig bei uns! Deine Aufgaben * Beratung unserer Kunden aus Pharma, Medizin und Wissenschaft * Konzeption und operative Umsetzung crossmedialer Maßnahmen * Projektmanagement mit Budgetverantwortung inkl. Projektcontrolling * Kommunikation und Abstimmung mit
med publico GmbH * Wiesbaden * Feste Anstellung * Vollzeit - Medizin, Gesundheit, Kommunikation – das ist seit 2007 unsere Leidenschaft. Du brennst für Deine Arbeit mit Kunden und möchtest Dich beruflich verändern? med publico ist eine medizinisch-wissenschaftliche Business Unit der wikonect GmbH. Wir beraten und betreuen führende Unternehmen und Institutionen aus der Pharmazeutischen Industrie und suchen Dich! Zur Verstärkung unseres bestehenden Teams mit mehr als 60 Mitarbeitenden suchen wir zum nächstmöglichen Zeitpunkt eine(n) Vollzeit, unbefristet - am Standort Wiesbaden - Du bist unkonventionell, ideenreich und liebst Deinen Beruf. – Dann bist Du genau richtig bei uns! Deine Aufgaben * Beratung unserer Kunden aus Pharma, Medizin und Wissenschaft * Konzeption und operative Umsetzung crossmedialer Maßnahmen * Projektmanagement mit Budgetverantwortung inkl. Projektcontrolling * Kommunikation und Abstimmung mit
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Postdoctoral Scientist in Subcellular Engineering (f/m/d)
Postdoctoral Scientist in Subcellular Engineering (f/m/d)
Max-Planck-Institut für Biophysik
Frankfurt am Main
Max-Planck-Institut für Biophysik * Frankfurt am Main * Befristeter Vertrag * Vollzeit - The Max Planck Institute of Biophysics is a leading international research center that develops biophysical, biochemical and computational methods to investigate the structure, dynamics and function of cellular systems at molecular scale. It consists of about 200 employees from more than 25 countries, and is located at the Campus Riedberg in Frankfurt am Main. Within the Department of Molecular Sociology, led by Martin Beck, we investigate large macromolecular assemblies using state-of-the-art in situ structural biology. Our work spans nuclear transport systems, protein complex assembly, protein homeostasis, and membrane protein complexes and membrane remodeling, as well as in situ studies of viruses, including SARS-CoV-2 and virus-like particles.
Max-Planck-Institut für Biophysik * Frankfurt am Main * Befristeter Vertrag * Vollzeit - The Max Planck Institute of Biophysics is a leading international research center that develops biophysical, biochemical and computational methods to investigate the structure, dynamics and function of cellular systems at molecular scale. It consists of about 200 employees from more than 25 countries, and is located at the Campus Riedberg in Frankfurt am Main. Within the Department of Molecular Sociology, led by Martin Beck, we investigate large macromolecular assemblies using state-of-the-art in situ structural biology. Our work spans nuclear transport systems, protein complex assembly, protein homeostasis, and membrane protein complexes and membrane remodeling, as well as in situ studies of viruses, including SARS-CoV-2 and virus-like particles.