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1.160 Treffer für Clinical Study Jobs
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Wissenschaftliche Mitarbeit (m/w/d) im Drittmittelprojekt - Deutsches Zentrum für Psychische Gesundheit
Wissenschaftliche Mitarbeit (m/w/d) im Drittmittelprojekt - Deutsches Zentrum für Psychische Gesundheit
Ruhr-Universität Bochum
Bochum
Ruhr-Universität Bochum * Bochum * Befristeter Vertrag * Teilzeit - Sei einer der ersten Bewerber - Wir suchen zum nächstmöglichen Zeitpunkt befristet in Teilzeit (29,87 Std./Woche = 75 %) eine*n - Das Deutsche Zentrum für Psychische Gesundheit (DZPG, dzpg.org) ist ein Netzwerk aus Hochschulen, Universitätskliniken und außeruniversitären Forschungseinrichtungen an sechs Standorten in Deutschland und Teil des Gesundheitsforschungsprogramms der Bundesregierung. Das DZPG verfolgt einen konsequent partizipativen Forschungsansatz sowie eine gelebte Open-Science-Policy. Gemeinsames Ziel ist es, psychische Erkrankungen besser zu verstehen, frühzeitig zu erkennen, wirksam zu behandeln und ihrer Entstehung vorzubeugen. Das Forschungs- und Behandlungszentrum für psychische Gesundheit (FBZ, fbz-bochum.de) der Ruhr-Universität Bochum ist ein Partnerstandort des DZPG und vereint Forschung, ...
Ruhr-Universität Bochum * Bochum * Befristeter Vertrag * Teilzeit - Sei einer der ersten Bewerber - Wir suchen zum nächstmöglichen Zeitpunkt befristet in Teilzeit (29,87 Std./Woche = 75 %) eine*n - Das Deutsche Zentrum für Psychische Gesundheit (DZPG, dzpg.org) ist ein Netzwerk aus Hochschulen, Universitätskliniken und außeruniversitären Forschungseinrichtungen an sechs Standorten in Deutschland und Teil des Gesundheitsforschungsprogramms der Bundesregierung. Das DZPG verfolgt einen konsequent partizipativen Forschungsansatz sowie eine gelebte Open-Science-Policy. Gemeinsames Ziel ist es, psychische Erkrankungen besser zu verstehen, frühzeitig zu erkennen, wirksam zu behandeln und ihrer Entstehung vorzubeugen. Das Forschungs- und Behandlungszentrum für psychische Gesundheit (FBZ, fbz-bochum.de) der Ruhr-Universität Bochum ist ein Partnerstandort des DZPG und vereint Forschung, ...
Wissenschaftliche Mitarbeit (m/w/d) im Drittmittelprojekt - Deutsches Zentrum für Psychische Gesundheit
Wissenschaftliche Mitarbeit (m/w/d) im Drittmittelprojekt - Deutsches Zentrum für Psychische Gesundheit
Ruhr-Universität Bochum
Bochum
Ruhr-Universität Bochum * Bochum * Befristeter Vertrag * Teilzeit - Sei einer der ersten Bewerber - Die Ruhr-Universität Bochum (RUB) ist eine der führenden Forschungsuniversitäten in Deutschland. Als reformorientierte Campusuniversität vereint sie in einzigartiger Weise die gesamte Spannbreite der großen Wissenschaftsbereiche an einem Ort. Das dynamische Miteinander von Fächern und Fächerkulturen bietet den Forschenden wie den Studierenden gleichermaßen besondere Chancen zur interdisziplinären Zusammenarbeit. Forschungs- und Behandlungszentrum für Psychische Gesundheit (FBZ) Deutsches Zentrum für Psychische Gesundheit (DZPG) Wir suchen zum nächstmöglichen Zeitpunkt befristet in Teilzeit (29,87 Std./Woche = 75 %) eine*n - Das Deutsche Zentrum für Psychische Gesundheit (DZPG, dzpg.org) ist ein Netzwerk aus Hochschulen, Universitätskliniken und außeruniversitären ...
Ruhr-Universität Bochum * Bochum * Befristeter Vertrag * Teilzeit - Sei einer der ersten Bewerber - Die Ruhr-Universität Bochum (RUB) ist eine der führenden Forschungsuniversitäten in Deutschland. Als reformorientierte Campusuniversität vereint sie in einzigartiger Weise die gesamte Spannbreite der großen Wissenschaftsbereiche an einem Ort. Das dynamische Miteinander von Fächern und Fächerkulturen bietet den Forschenden wie den Studierenden gleichermaßen besondere Chancen zur interdisziplinären Zusammenarbeit. Forschungs- und Behandlungszentrum für Psychische Gesundheit (FBZ) Deutsches Zentrum für Psychische Gesundheit (DZPG) Wir suchen zum nächstmöglichen Zeitpunkt befristet in Teilzeit (29,87 Std./Woche = 75 %) eine*n - Das Deutsche Zentrum für Psychische Gesundheit (DZPG, dzpg.org) ist ein Netzwerk aus Hochschulen, Universitätskliniken und außeruniversitären ...
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Schnelle Bewerbung
Review and provide scientific input on clinical data–related documents, including statistical analysis plans (SAPs), tables, listings, and figures (TLFs), and clinical study reports (CSRs). Actively contribute to clinical development strategy, including benefit–risk assessments, study optimization, interpretation of emerging data, and program-level decision-making processes. * Provide scientific guidance on clinical study design, including definition of study objectives, endpoints, eligibility criteria, and key statistical considerations, in close collaboration with the Clinical Operations team. As a manufacturer of Advanced Therapy Medicinal Products (ATMPs) in accordance with Section 13 of the German Medicines Act (AMG), we develop and produce proprietary cell therapeutics that are currently in late-stage clinical trials that are currently in late-stage clinical trials.
Review and provide scientific input on clinical data–related documents, including statistical analysis plans (SAPs), tables, listings, and figures (TLFs), and clinical study reports (CSRs). Actively contribute to clinical development strategy, including benefit–risk assessments, study optimization, interpretation of emerging data, and program-level decision-making processes. * Provide scientific guidance on clinical study design, including definition of study objectives, endpoints, eligibility criteria, and key statistical considerations, in close collaboration with the Clinical Operations team. As a manufacturer of Advanced Therapy Medicinal Products (ATMPs) in accordance with Section 13 of the German Medicines Act (AMG), we develop and produce proprietary cell therapeutics that are currently in late-stage clinical trials that are currently in late-stage clinical trials.
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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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The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information
The Clinical Study Administrator (CSA) assists in the coordination of study activities from the start up to execution and close out within Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good Clinical Practices (GCP), Alexion Standard Operating Procedures (SOPs) and evolving regulatory requirements. The CSA collaborates closely with the Country Operations (PMCO) and other local study team members in COM such as Study Start Up (SSU) manager, Clinical Research Associates (CRA), Site Management Leads (SML) and Head of Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. * Collaborating with PMCO, CRAs, SSU manager and study vendors on the preparation, supports the handling and distribution of clinical trial supplies and maintenance of tracking information
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You contribute with value and actively drive the workflow solution concept in product generation projects, in (early) innovation projects as well as in clinical or medical studies * As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution * You own our applicative and clinical understanding of cranial tumor microsurgery procedures, you observe current trends and developments in clinics and industry * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in cranial tumor microsurgery * You establish and maintain a close customer interface in spine clinical environment * At least 8 years of professional experience in the medical industry or in a clinical environment
You contribute with value and actively drive the workflow solution concept in product generation projects, in (early) innovation projects as well as in clinical or medical studies * As a Senior Product Portfolio Manager (f/m/x) within ZEISS Meditec AG, your role is similar to and in strong collaboration with product management for the single products contributing to your clinical workflow solution * You own our applicative and clinical understanding of cranial tumor microsurgery procedures, you observe current trends and developments in clinics and industry * You propose and evaluate attractive potential future offerings to drive clinical outcome or clinical workflow improvement in cranial tumor microsurgery * You establish and maintain a close customer interface in spine clinical environment * At least 8 years of professional experience in the medical industry or in a clinical environment
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Profil is a globally leading contract research organization (CRO) specializing in clinical studies for metabolic diseases such as diabetes, obesity, and related disorders. For more than 25 years, Profil has been a trusted partner to pharmaceutical and biotechnology companies worldwide, known for scientific excellence, innovative study designs, and in early-phase outstanding data quality clinical development. * Solid understanding of clinical development, ideally early-phase (Phase 1–2)
Profil is a globally leading contract research organization (CRO) specializing in clinical studies for metabolic diseases such as diabetes, obesity, and related disorders. For more than 25 years, Profil has been a trusted partner to pharmaceutical and biotechnology companies worldwide, known for scientific excellence, innovative study designs, and in early-phase outstanding data quality clinical development. * Solid understanding of clinical development, ideally early-phase (Phase 1–2)
Schnelle Bewerbung
We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. * Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. * Proper handling, accountability and reconciliation of investigational products and clinical supplies. * Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. * Preparefor and participatein onsite study audits or regulatory agency inspections. * Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.
We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. * Accurate and timely data entry into study specific EDC systems and timely resolution of data clarification queries issued for the site. * Proper handling, accountability and reconciliation of investigational products and clinical supplies. * Scheduleand/or performstudy procedures as per study requirements and delegation of responsibilities. * Preparefor and participatein onsite study audits or regulatory agency inspections. * Flexibility in working hours may be required depending on the schedule of study procedures and/or patient visits.
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Studienassistenz (Study Nurse) im Studienzentrum (m/w/d) in Siegen bei Diakonie in Südwestfalen gGmbH
Studienassistenz (Study Nurse) im Studienzentrum (m/w/d) in Siegen bei Diakonie in Südwestfalen gGmbH
Diakonie Klinikum GmbH
57 Siegen, Deutschland
erfolgte oder geplante Weiterbildung Studienassistenz / Study Nurse
erfolgte oder geplante Weiterbildung Studienassistenz / Study Nurse
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Clinical Research Associate / Senior Clinical Research Associate
Clinical Research Associate / Senior Clinical Research Associate
PSI CRO Deutschland GmbH
Munich
Teilweise Home-Office
Schnelle Bewerbung
As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. * Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
As a Senior / Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. * Independent experience in all types of monitoring visits in AMG studies, Phases II and/or III.
Schnelle Bewerbung
Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents * Prepare for and attend internal and external study audits pertinent to Statistics * Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, and draw conclusions from complex statistical information - You will contribute to statistical activities related to global clinical trials and work closely with international teams of , and , including the role of biostatistics project lead * Conduct statistical analysis for clinical trials including, interim analysis, final analysis, analysis for DSMBs/DMCs and PK analysis * Develop and review study protocols, statistical analysis plans, analysis dataset specifications according to CDISC ADaM standard and other project-specific documents * Prepare for and attend internal and external study audits pertinent to Statistics * Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research
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As a Project Manager in the Clinical Operations team you will independently oversee (inter-)national clinical drug trials, non-interventional studies, medical-device studies and IT-related research projects of high complexity. This role blends traditional clinical project management with the operational coordination of digital tools, platforms and IT services used in patient-centric studies. * Serve as the primary point of contact for the sponsor and drive project planning, execution and timelines - from study-start activities through ongoing study management to the coordination of all phases of the clinical-trial lifecycle. * Coordinate and manage IT services and platforms that support clinical studies (e.g., ePRO, eCOA, eCRF, patient-engagement tools). * Preferably you have experience with non-interventional studies (NIS) as well as clinical trials.
As a Project Manager in the Clinical Operations team you will independently oversee (inter-)national clinical drug trials, non-interventional studies, medical-device studies and IT-related research projects of high complexity. This role blends traditional clinical project management with the operational coordination of digital tools, platforms and IT services used in patient-centric studies. * Serve as the primary point of contact for the sponsor and drive project planning, execution and timelines - from study-start activities through ongoing study management to the coordination of all phases of the clinical-trial lifecycle. * Coordinate and manage IT services and platforms that support clinical studies (e.g., ePRO, eCOA, eCRF, patient-engagement tools). * Preferably you have experience with non-interventional studies (NIS) as well as clinical trials.
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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.
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Medizinische Fachangestellte / Study Nurse / Clinical Research Assistant (m/w/d)
Medizinische Fachangestellte / Study Nurse / Clinical Research Assistant (m/w/d)
Universitätsklinikum Bonn
Bonn
Teilweise Home-Office
Schnelle Bewerbung
Vorhandene Zusatzbezeichnung Study Nurse (m/w/d) oder ähnliche Qualifikationen wie z. B. Dokumentationsassistenz oder Interesse, diese zu erwerben * Weiterbildung zur Study Nurse, falls sie MFA sind
Vorhandene Zusatzbezeichnung Study Nurse (m/w/d) oder ähnliche Qualifikationen wie z. B. Dokumentationsassistenz oder Interesse, diese zu erwerben * Weiterbildung zur Study Nurse, falls sie MFA sind
Schnelle Bewerbung
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML collaborates with Clinical Research teams and serves as a key liaison between Clinical Research and Global Safety teams. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. ML drives execution for assigned projects in collaboration with Clinical Research teams and other cross-functional stakeholders. * Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML collaborates with Clinical Research teams and serves as a key liaison between Clinical Research and Global Safety teams. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. ML drives execution for assigned projects in collaboration with Clinical Research teams and other cross-functional stakeholders. * Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents
NEU
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Clinical Research Associate / Junior Monitor klinische Studien (m/w/d)
Clinical Research Associate / Junior Monitor klinische Studien (m/w/d)
wu personal GmbH
bundesweit, Home-Office
Teilweise Home-Office
Für unseren Auftraggeber, ein führendes, globales Unternehmen in der Medizintechnologie-Branche, suchen wir mehrere Mitarbeiter als Clinical Research Associate / Junior Monitor (m/w/d) für das Monitoring klinischer Studien. * Durchführung von Monitoring-Aktivitäten gemäß Prüfplan bzw. Monitoring-Plan, Standardarbeitsanweisungen guter klinischer Praxis (Good Clinical Practice) und regulatorischen Vorgaben * Identifikation, Dokumentation und Eskalation von Protokollabweichungen, Daten-Diskrepanzen und Nichtkonformität (Non-Compliance) an Monitoring-Management und Study Team gemäß Eskalationswegen * Nachweisbare Berufserfahrung im klinischen Monitoring (Clinical Research Monitoring), idealerweise 1 bis 3 Jahre
Für unseren Auftraggeber, ein führendes, globales Unternehmen in der Medizintechnologie-Branche, suchen wir mehrere Mitarbeiter als Clinical Research Associate / Junior Monitor (m/w/d) für das Monitoring klinischer Studien. * Durchführung von Monitoring-Aktivitäten gemäß Prüfplan bzw. Monitoring-Plan, Standardarbeitsanweisungen guter klinischer Praxis (Good Clinical Practice) und regulatorischen Vorgaben * Identifikation, Dokumentation und Eskalation von Protokollabweichungen, Daten-Diskrepanzen und Nichtkonformität (Non-Compliance) an Monitoring-Management und Study Team gemäß Eskalationswegen * Nachweisbare Berufserfahrung im klinischen Monitoring (Clinical Research Monitoring), idealerweise 1 bis 3 Jahre
NEU
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Study Nurse / Studienassistenz / Gesundheits- und Krankenpfleger / MFA (m/w/d)
Study Nurse / Studienassistenz / Gesundheits- und Krankenpfleger / MFA (m/w/d)
Universitätsklinikum Ulm
Ulm
Kenntnisse der gesetzlichen Anforderungen im Bereich klinischer Prüfungen und Good Clinical Practice (GCP) wünschenswert
Kenntnisse der gesetzlichen Anforderungen im Bereich klinischer Prüfungen und Good Clinical Practice (GCP) wünschenswert
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Project Manager Pre-Clinical Research / Toxicology (m/f/d)
Project Manager Pre-Clinical Research / Toxicology (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
In this scientifically oriented position, you will be responsible for the oversight, and evaluation of preclinical and toxicological studies. * Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research * Comprehensive data interpretation, including assessment of pharmacological and toxicological endpoints, integration of findings across studies, and development of scientifically substantiated conclusions * Evaluation of study reports and scientific summaries, ensuring accuracy, transparency, and regulatory compliance * In‑depth understanding of regulatory requirements for preclinical studies (e.g., GLP, ICH, OECD guidelines)
In this scientifically oriented position, you will be responsible for the oversight, and evaluation of preclinical and toxicological studies. * Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research * Comprehensive data interpretation, including assessment of pharmacological and toxicological endpoints, integration of findings across studies, and development of scientifically substantiated conclusions * Evaluation of study reports and scientific summaries, ensuring accuracy, transparency, and regulatory compliance * In‑depth understanding of regulatory requirements for preclinical studies (e.g., GLP, ICH, OECD guidelines)
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Klinische*r Studienkoordinator*in (m/w/d) / Study Nurse (m/w/d) für Investigator Initiated Trials - AG Translationale Pharmakologie
Klinische*r Studienkoordinator*in (m/w/d) / Study Nurse (m/w/d) für Investigator Initiated Trials - AG Translationale Pharmakologie
Universität Bielefeld
Bielefeld
Teilweise Home-Office
Sie übernehmen die klinische Studienkoordination als Study Nurse. * zertifizierte Qualifizierung zur Study Nurse / Studienassistent*in / Studien Koordinator*in * zertifizierte Weiterbildung in Good Clinical Practice
Sie übernehmen die klinische Studienkoordination als Study Nurse. * zertifizierte Qualifizierung zur Study Nurse / Studienassistent*in / Studien Koordinator*in * zertifizierte Weiterbildung in Good Clinical Practice
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Senior Clinical Research Associate (CRA) (m/w/d)
Senior Clinical Research Associate (CRA) (m/w/d)
GBG Forschungs GmbH
Neu-Isenburg bei Frankfurt am Main
Teilweise Home-Office
Als Sr. Clinical Research Associate übernehmen Sie eine Schlüsselrolle in der erfolgreichen Durchführung klinischer Studien. * Bei Bedarf und separater Zuweisung; Agieren als Study Lead für internationale und nationale Studien * Weiterbildung im Bereich CRA, sowie mehrjährige Erfahrung als Clinical Research Associate
Als Sr. Clinical Research Associate übernehmen Sie eine Schlüsselrolle in der erfolgreichen Durchführung klinischer Studien. * Bei Bedarf und separater Zuweisung; Agieren als Study Lead für internationale und nationale Studien * Weiterbildung im Bereich CRA, sowie mehrjährige Erfahrung als Clinical Research Associate
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Studienassistenz / Study Nurse Reise- und Tropenmedizin (w/m/d)
Studienassistenz / Study Nurse Reise- und Tropenmedizin (w/m/d)
Universitätsklinikum Tübingen
Tübingen
Teilweise Home-Office
Die Clinical Trial Platform befasst sich hauptsächlich mit klinischen Studien zur Erforschung neuer Medikamente und Impfstoffe zur Therapie und Prävention von Infektionskrankheiten in Tübingen und am Partnerinstitut in Lambaréné, Gabun. * Zusatzqualifikation als Studienassistenz / Study Nurse
Die Clinical Trial Platform befasst sich hauptsächlich mit klinischen Studien zur Erforschung neuer Medikamente und Impfstoffe zur Therapie und Prävention von Infektionskrankheiten in Tübingen und am Partnerinstitut in Lambaréné, Gabun. * Zusatzqualifikation als Studienassistenz / Study Nurse
Schnelle Bewerbung
Sie arbeiten eng mit Commercial, Finance, Data Protection, Study Management sowie mit externen Rechtsanwälten zusammen und agieren als zentrale kommerzielle Schnittstelle für alle vertraglichen Themen gegenüber unseren internationalen Kunden. * Verantwortung für den gesamten Vertragslebenszyklus von klinischen Studienverträgen (z. B. Master Service Agreements, Clinical Trial Agreements, Vendor- and Service Agreements)
Sie arbeiten eng mit Commercial, Finance, Data Protection, Study Management sowie mit externen Rechtsanwälten zusammen und agieren als zentrale kommerzielle Schnittstelle für alle vertraglichen Themen gegenüber unseren internationalen Kunden. * Verantwortung für den gesamten Vertragslebenszyklus von klinischen Studienverträgen (z. B. Master Service Agreements, Clinical Trial Agreements, Vendor- and Service Agreements)
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Studienvorbereitung: Pre-Study-Visits, Zusammenstellung essenzieller Dokumente nach Anforderung des Prüfplans * Kommunikation mit nationalen Studienzentralen und internationalen Clinical Research Organisationen * Bereitschaft zur kontinuierlichen Fort- und Weiterbildung (Good Clinical Practice (GCP), IATA) sowie Teilnahme an Studientreffen
Studienvorbereitung: Pre-Study-Visits, Zusammenstellung essenzieller Dokumente nach Anforderung des Prüfplans * Kommunikation mit nationalen Studienzentralen und internationalen Clinical Research Organisationen * Bereitschaft zur kontinuierlichen Fort- und Weiterbildung (Good Clinical Practice (GCP), IATA) sowie Teilnahme an Studientreffen
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Wissenschaftlicher Koordinator / Projektmanager (m/w/d)
Wissenschaftlicher Koordinator / Projektmanager (m/w/d)
Deutsches Krebsforschungszentrum DKFZ
Heidelberg
Teilweise Home-Office
Für das Clinical Trial Center (CTC) Heidelberg des NCT Heidelberg suchen wir ab Mai 2026 eine:n Wissenschaftliche:n Koordinator:in / Projektmanager:in (m/w/d). * Schnittstellenmanagement beim Study-Start-up: Sie sind die zentrale Ansprechperson für externe Parteien (Sponsoren, CROs, akademische Netzwerke etc.), Studienteams und interne Kooperationspartner
Für das Clinical Trial Center (CTC) Heidelberg des NCT Heidelberg suchen wir ab Mai 2026 eine:n Wissenschaftliche:n Koordinator:in / Projektmanager:in (m/w/d). * Schnittstellenmanagement beim Study-Start-up: Sie sind die zentrale Ansprechperson für externe Parteien (Sponsoren, CROs, akademische Netzwerke etc.), Studienteams und interne Kooperationspartner
Our goal is to comprehensively study the impact of gene fusions and other genetic drivers in sarcomagenesis, uncover specific vulnerabilities they create, and ultimately aim at maximizing the potential for rapid clinical translation. The Division of Soft-Tissue Sarcoma at DKFZ applies cutting-edge technology to study and dissect the underlying molecular mechanisms in many types of soft-tissue sarcomas, where chromosomal translocations generate fusion oncoproteins that serve as drivers of the disease.
Our goal is to comprehensively study the impact of gene fusions and other genetic drivers in sarcomagenesis, uncover specific vulnerabilities they create, and ultimately aim at maximizing the potential for rapid clinical translation. The Division of Soft-Tissue Sarcoma at DKFZ applies cutting-edge technology to study and dissect the underlying molecular mechanisms in many types of soft-tissue sarcomas, where chromosomal translocations generate fusion oncoproteins that serve as drivers of the disease.