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- Frankfurt am Main
- Köln
- Düsseldorf
- Dortmund
- Essen
- Münster, Nordrhein-Westfalen
- Bonn
- Duisburg
- Aachen
- Wiesbaden
- Bochum
- Mainz
- Koblenz
- Gießen
- Kaiserslautern
- Bergisch Gladbach
- Eschborn
- Bad Homburg vor der Höhe
- Neu-Isenburg
- Hürth
- Europa
- Westliches Europa
- Westdeutschland
- Nordrhein-Westfalen
- Rheinland
- Hessen
- Ruhrgebiet
- Niederrhein
- Rheinland-Pfalz
- Münsterland
- Bergisches Land
238 Treffer für Clinical Study Jobs in Westdeutschland im Umkreis von 30 km
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Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest. * Assess clinical study ideas and initiatives as well as act as for the respective internal approval process. * Define data endpoints and sample sizes (together with clinical evaluation team and support of biostatistics) for data collections, studies and clinical initiatives. * Author and review study synopses and clinical trial protocols, regulatory documents, and study-related publications for clinical initiatives and grants. * Several years' experience in clinical and scientific research (especially in study designs and scientific research questions) To enlarge our Clinical Regulatory Affairs Team we are looking as soon as possible for a * Give insights into clinical data sets and evidence for our company's products to internal stakeholders.
Develop clinical trial strategies, shaping study designs based on regulatory requirements, competitive insights and company's research interest. * Assess clinical study ideas and initiatives as well as act as for the respective internal approval process. * Define data endpoints and sample sizes (together with clinical evaluation team and support of biostatistics) for data collections, studies and clinical initiatives. * Author and review study synopses and clinical trial protocols, regulatory documents, and study-related publications for clinical initiatives and grants. * Several years' experience in clinical and scientific research (especially in study designs and scientific research questions) To enlarge our Clinical Regulatory Affairs Team we are looking as soon as possible for a * Give insights into clinical data sets and evidence for our company's products to internal stakeholders.
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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 * 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 * 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 ...
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 * 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 * 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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(Senior) Regulatory Affairs Manager (m/w/d)
(Senior) Regulatory Affairs Manager (m/w/d)
Profil Institut für Stoffwechselforschung GmbH
Neuss
Teilweise Home-Office
Profil Institut für Stoffwechselforschung GmbH * Neuss * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Profil ist ein 1999 gegründetes, international tätiges und renommiertes Auftragsforschungsinstitut im Bereich der Stoffwechselerkrankungen. Wir arbeiten seit vielen Jahren gemeinsam mit der Pharmaindustrie an der Entwicklung neuer Arzneimittel für die Behandlung von Diabetes, Adipositas und damit einhergehenden Erkrankungen. Auch die Weiterentwicklung bekannter Wirkstoffe sowie der technischen Möglichkeiten zur Verabreichung von Insulin und der Messung der Blutzuckerkonzentration wird von uns intensiv unterstützt. Aufgrund unserer jahrelangen Erfahrungen konnten wir umfassendes wissenschaftliches Know-how und einzigartige Expertise im Bereich der Stoffwechselerkrankungen aufbauen.
Profil Institut für Stoffwechselforschung GmbH * Neuss * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Profil ist ein 1999 gegründetes, international tätiges und renommiertes Auftragsforschungsinstitut im Bereich der Stoffwechselerkrankungen. Wir arbeiten seit vielen Jahren gemeinsam mit der Pharmaindustrie an der Entwicklung neuer Arzneimittel für die Behandlung von Diabetes, Adipositas und damit einhergehenden Erkrankungen. Auch die Weiterentwicklung bekannter Wirkstoffe sowie der technischen Möglichkeiten zur Verabreichung von Insulin und der Messung der Blutzuckerkonzentration wird von uns intensiv unterstützt. Aufgrund unserer jahrelangen Erfahrungen konnten wir umfassendes wissenschaftliches Know-how und einzigartige Expertise im Bereich der Stoffwechselerkrankungen aufbauen.
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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
Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. Die Stelle ist dem Clinical Development Team * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. Die Stelle ist dem Clinical Development Team * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
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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. * 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 - 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
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. * 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 - 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
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Senior Clinical Trial Physician (m|f|d)
Senior Clinical Trial Physician (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
You will review and analyze clinical trial data, contributing to Clinical Study Reports (CSRs), MAA/BLA submissions, and other regulatory documentation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As a Senior Clinical Trial Physician, you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning, execution, and supervision of clinical trials in hemato-oncology.
You will review and analyze clinical trial data, contributing to Clinical Study Reports (CSRs), MAA/BLA submissions, and other regulatory documentation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As a Senior Clinical Trial Physician, you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning, execution, and supervision of clinical trials in hemato-oncology.
Group Leader – Clinical Operational Excellence (m|f|d)
Group Leader – Clinical Operational Excellence (m|f|d)
Miltenyi Biotec B.V. & Co. KG
Bergisch Gladbach
Teilweise Home-Office
Together with your team you will oversee TMF services, trial oversight- and training requirements for clinical studies, including Key Peformance Indicator management, TMF vendor oversight, and proactive risk mitigation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As Group Leader – Clinical Operational Excellence, you will lead a team of and take ownership of driving operational excellence across our European Clinical Development organization. * You will lead and coordinate clinical operational excellence initiatives including inspection readiness initiatives across ...
Together with your team you will oversee TMF services, trial oversight- and training requirements for clinical studies, including Key Peformance Indicator management, TMF vendor oversight, and proactive risk mitigation. We are pioneering groundbreaking therapies for serious life-threatening diseases, and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend patients' lives. Our lead candidate, a tandem CAR-T cell product, is currently undergoing pivotal clinical trials on a global scale. As Group Leader – Clinical Operational Excellence, you will lead a team of and take ownership of driving operational excellence across our European Clinical Development organization. * You will lead and coordinate clinical operational excellence initiatives including inspection readiness initiatives across ...
Noch nichts dabei? Es gibt 231 weitere Jobs, die zu deiner Suche passen könnten
Die klinische Studiengruppe besteht derzeit aus 3 Study Nurses, einem Studienarzt sowie einigen studentischen Hilfskräften. * Vorkenntnisse/Qualifikation in GCP (good clinical practice) wünschenswert
Die klinische Studiengruppe besteht derzeit aus 3 Study Nurses, einem Studienarzt sowie einigen studentischen Hilfskräften. * Vorkenntnisse/Qualifikation in GCP (good clinical practice) wünschenswert
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PhD Student (f/m/x) in Molecular Epidemiology
PhD Student (f/m/x) in Molecular Epidemiology
Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (DZNE)
Bonn
The Rhineland Study includes comprehensive multi-omics data, including (epi)genomics, transcriptomics, metabolomics, lipidomics, and proteomics, advanced MRI data, as well as extensive behavioral and clinical data, including cognitive and neurological assessments, cardiovascular and anthropometric assessments, sensory systems tests, medical history, and medication use. The project will leverage large-scale population-based cohorts, in particular the Rhineland Study, which is spearheaded by Prof. Dr. Dr. Monique M. B. Breteler. The study currently includes over 12,500 individuals, nearly 5,000 of whom already have longitudinal data. * Experience with epidemiological research or large-scale observational studies, particularly involving omics or brain imaging data
The Rhineland Study includes comprehensive multi-omics data, including (epi)genomics, transcriptomics, metabolomics, lipidomics, and proteomics, advanced MRI data, as well as extensive behavioral and clinical data, including cognitive and neurological assessments, cardiovascular and anthropometric assessments, sensory systems tests, medical history, and medication use. The project will leverage large-scale population-based cohorts, in particular the Rhineland Study, which is spearheaded by Prof. Dr. Dr. Monique M. B. Breteler. The study currently includes over 12,500 individuals, nearly 5,000 of whom already have longitudinal data. * Experience with epidemiological research or large-scale observational studies, particularly involving omics or brain imaging data
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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. The German entity in Mainz is responsible for key development tasks including sensor design, chemistry validation, system evaluation and data analysis from both laboratory and patient studies. 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. * Completed studies (Bachelor or Master) in bioinformatics or a completed scientific degree in a comparable scientific degree in a comparable subject and knowledge of computer science
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. The German entity in Mainz is responsible for key development tasks including sensor design, chemistry validation, system evaluation and data analysis from both laboratory and patient studies. 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. * Completed studies (Bachelor or Master) in bioinformatics or a completed scientific degree in a comparable scientific degree in a comparable subject and knowledge of computer science
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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. * Strong background in assessing primary packaging interactions with products, supported by experience in extractables and leachable studies.
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. * Strong background in assessing primary packaging interactions with products, supported by experience in extractables and leachable studies.
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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 interests and is consistent with ICON's rules, procedures, and policies. 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 ...
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 interests and is consistent with ICON's rules, procedures, and policies. 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 ...
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Technical Assistant (BTA) (m/f/d) (full-time position 100 % ~ 38,5 h/week)
Technical Assistant (BTA) (m/f/d) (full-time position 100 % ~ 38,5 h/week)
Universitätsklinikum Bonn
Bonn
Around 3,500 students study medicine and dentistry here, and over 600 people are trained annually in healthcare professions. Prof. Boztug's research program bridges fundamental discoveries in immune dysregulation with clinical translation. The group employs a combination of model organism research, including zebrafish and mouse models, together with translational approaches, enabling detailed study of the molecular and cellular processes driving immune dysfunction.
Around 3,500 students study medicine and dentistry here, and over 600 people are trained annually in healthcare professions. Prof. Boztug's research program bridges fundamental discoveries in immune dysregulation with clinical translation. The group employs a combination of model organism research, including zebrafish and mouse models, together with translational approaches, enabling detailed study of the molecular and cellular processes driving immune dysfunction.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. * Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. 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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. * Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. 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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
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With over 2000 m² of lab space across France and Germany, we offer comprehensive services in bio-prediction, preclinical efficacy evaluation, and clinical trials. QIMA Monasterium is based in Münster, Germany, and specializes in pre-clinical and clinical services in dermatology for therapeutics, cosmeceutical, and nutraceutical applications, offering among other clinically relevant ex vivo and in vivo pre-clinical models and state-of-the-art techniques. We are seeking a team-orientated and highly motivated Business Development Managers (m/f/d) full-time to join our international team, while having the specialization and focus on QIMA Monasterium service offering in clinical ex vivo and in-vivo pre-clinical models. * Develop study proposals (with the support of the scientific team) and negotiate with clients, * Interact in inter-department cooperation to obtain the most efficient teamwork ...
With over 2000 m² of lab space across France and Germany, we offer comprehensive services in bio-prediction, preclinical efficacy evaluation, and clinical trials. QIMA Monasterium is based in Münster, Germany, and specializes in pre-clinical and clinical services in dermatology for therapeutics, cosmeceutical, and nutraceutical applications, offering among other clinically relevant ex vivo and in vivo pre-clinical models and state-of-the-art techniques. We are seeking a team-orientated and highly motivated Business Development Managers (m/f/d) full-time to join our international team, while having the specialization and focus on QIMA Monasterium service offering in clinical ex vivo and in-vivo pre-clinical models. * Develop study proposals (with the support of the scientific team) and negotiate with clients, * Interact in inter-department cooperation to obtain the most efficient teamwork ...
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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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Medizinischer Fachangestellter/MFA als Study Nurse (gn*) Augenklinik
Medizinischer Fachangestellter/MFA als Study Nurse (gn*) Augenklinik
UKM Universitätsklinikum Münster
Münster
Zusätzliche Qualifikation als Study Nurse (gn*) und/oder Erfahrung in der Betreuung klinischer Studien von Vorteil
Zusätzliche Qualifikation als Study Nurse (gn*) und/oder Erfahrung in der Betreuung klinischer Studien von Vorteil
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Organisation von Monitorbesuchen, Initiierungen, Pre-Study Visits, Audits
Organisation von Monitorbesuchen, Initiierungen, Pre-Study Visits, Audits
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In der globalen Schlüsselrolle als Clinical Expert R&D (m/w/d) leisten Sie einen entscheidenden Beitrag zur Entwicklung von Medizinprodukten im orthopädischen Bereich - Produkte, die der Markt benötigt. * Als Schnittstelle zwischen Abteilungen wie Clinical Development, Market-Driven Innovation, Technical Development und Regulatory Affairs koordinieren Sie Informationen und treiben Projekte in den ersten Entwicklungsphasen effizient voran. * Als Clinical Expert R&D fungieren Sie intern als zentrale Ansprechperson für alle klinisch-wissenschaftlichen Fragestellungen in der Abteilung für Produktneuentwicklung.
In der globalen Schlüsselrolle als Clinical Expert R&D (m/w/d) leisten Sie einen entscheidenden Beitrag zur Entwicklung von Medizinprodukten im orthopädischen Bereich - Produkte, die der Markt benötigt. * Als Schnittstelle zwischen Abteilungen wie Clinical Development, Market-Driven Innovation, Technical Development und Regulatory Affairs koordinieren Sie Informationen und treiben Projekte in den ersten Entwicklungsphasen effizient voran. * Als Clinical Expert R&D fungieren Sie intern als zentrale Ansprechperson für alle klinisch-wissenschaftlichen Fragestellungen in der Abteilung für Produktneuentwicklung.
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Digital Account Manager B2B - Studydrive (m/w/d)
Digital Account Manager B2B - Studydrive (m/w/d)
meinestadt.de
Köln, Erlangen, Berlin, Essen/Ruhr, Gießen, Leipzig
Teilweise Home-Office
Neukundenakquise: Du gewinnst neue Arbeitgeber als Kund:innen für unsere Marke Studydrive, indem du sie von unserer einzigartigen Mission überzeugst und darin berätst, wie sie die Fachkräfte von morgen von sich begeistern können. Dazu arbeitest du strategisch mit deinen :innen und verbindest die Herausforderungen mit den passenden Angeboten von Studydrive. * Du bringst Reisebereitschaft mit, um Bestandskunden zu besuchen oder Studydrive auf Veranstaltungen zu repräsentieren.
Neukundenakquise: Du gewinnst neue Arbeitgeber als Kund:innen für unsere Marke Studydrive, indem du sie von unserer einzigartigen Mission überzeugst und darin berätst, wie sie die Fachkräfte von morgen von sich begeistern können. Dazu arbeitest du strategisch mit deinen :innen und verbindest die Herausforderungen mit den passenden Angeboten von Studydrive. * Du bringst Reisebereitschaft mit, um Bestandskunden zu besuchen oder Studydrive auf Veranstaltungen zu repräsentieren.
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Studienzentrum Dr. med Keller * Frankfurt am Main * Feste Anstellung * Vollzeit - Studienzentrum Dr. Claus Keller - Unser Studienzentrum besteht seit 1995. Seit diesem Zeitpunkt führen wir große Antibiotika-Studien, Asthma- und COPD-Studien sowie Studien bezüglich Corona, Lungenentzündung, Grippe etc. erfolgreich von der Phase 1 B – 3 durch. Unsere Auftraggeber sind seit Jahren große amerikanische Pharmakonzerne. Im Rahmen der Studien bedienen wir Anforderungen, die Geschäftspartner und Gesetzgeber im In- und Ausland an uns stellen, zu 100 Prozent. Bei der Durchführung steht auf der einen Seite der Auftraggeber und auf der anderen Seite die Probanden im Focus. Unser Ziel ist es, beide Seiten zufriedenzustellen. Ihre Aufgaben im Rahmen unserer Studien * Sie organisieren und dokumentieren einzelne Schritte der Studien, treffen etwa eine Vorauswahl der Probanden und betreuen diese ...
Studienzentrum Dr. med Keller * Frankfurt am Main * Feste Anstellung * Vollzeit - Studienzentrum Dr. Claus Keller - Unser Studienzentrum besteht seit 1995. Seit diesem Zeitpunkt führen wir große Antibiotika-Studien, Asthma- und COPD-Studien sowie Studien bezüglich Corona, Lungenentzündung, Grippe etc. erfolgreich von der Phase 1 B – 3 durch. Unsere Auftraggeber sind seit Jahren große amerikanische Pharmakonzerne. Im Rahmen der Studien bedienen wir Anforderungen, die Geschäftspartner und Gesetzgeber im In- und Ausland an uns stellen, zu 100 Prozent. Bei der Durchführung steht auf der einen Seite der Auftraggeber und auf der anderen Seite die Probanden im Focus. Unser Ziel ist es, beide Seiten zufriedenzustellen. Ihre Aufgaben im Rahmen unserer Studien * Sie organisieren und dokumentieren einzelne Schritte der Studien, treffen etwa eine Vorauswahl der Probanden und betreuen diese ...
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Consultant Schnittstellen (m/w/d) für unsere Krankenhaussoftware iMedOne®
Consultant Schnittstellen (m/w/d) für unsere Krankenhaussoftware iMedOne®
TELEKOM HEALTHCARE SOLUTIONS Deutsche Telekom Clinical Solutions GmbH
Bensheim, Köln, Bochum
Teilweise Home-Office
Schnelle Bewerbung
TELEKOM HEALTHCARE SOLUTIONS Deutsche Telekom Clinical Solutions GmbH
TELEKOM HEALTHCARE SOLUTIONS Deutsche Telekom Clinical Solutions GmbH
Moderne Ausstattung mit interaktiven Tafeln, Nursing AnneTM und Clinical Key Student® Plattform
Moderne Ausstattung mit interaktiven Tafeln, Nursing AnneTM und Clinical Key Student® Plattform
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Anschreiben nicht erforderlich
Study Lunch - Zum Netzwerken und Austausch findet monatlich der Study Lunch gemeinsam mit anderen :innen und Praktikant:innen statt
Study Lunch - Zum Netzwerken und Austausch findet monatlich der Study Lunch gemeinsam mit anderen :innen und Praktikant:innen statt
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Escalations to senior Near Patient Team members including the Near Patient Nurse Team Lead and the Near Patient Physician Lead will be required based on the clinical findings. * Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the . * Be prepared to liaise with and patients, to obtain detailed clinical information including past medical history to allow for accurate on-going case management. * Establish and maintain the relationships with ; leveraging these relationships for clinical quality assurance and oversight
Escalations to senior Near Patient Team members including the Near Patient Nurse Team Lead and the Near Patient Physician Lead will be required based on the clinical findings. * Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the . * Be prepared to liaise with and patients, to obtain detailed clinical information including past medical history to allow for accurate on-going case management. * Establish and maintain the relationships with ; leveraging these relationships for clinical quality assurance and oversight
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