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66 Treffer für Clinical Trial Jobs in Südbayern im Umkreis von 30 km
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Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or sample metadata, and analysis outputs.
Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or sample metadata, and analysis outputs.
Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. * Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. * Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct ...
Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables. * Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities. * Reviews the project oversight dashboards and other clinical trial systems (e.g. Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs),Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct ...
NEU
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TUM Klinikum Rechts der Isar * München * Befristeter Vertrag * Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Ihr Universitätsklinikum im Herzen Münchens - Wir sind das TUM Klinikum Rechts der Isar und verlässlicher Arbeitgeber für rund 6.600 Mitarbeiter*innen. Als Uniklinikum widmen wir uns neben der Krankenversorgung auch der Forschung und Lehre – entsprechend unserem Leitbild „Wissenschaft Heilung“ und genießen national wie international einen ausgezeichneten Ruf. 160 unterschiedliche Berufsgruppen arbeiten Hand in Hand, um unseren Patient*innen eine optimale Behandlung zukommen zu lassen. Voll- und Teilzeit | befristet (12 Monate) * Sie übernehmen die Koordination und die Begleitung von Vertragsverhandlungen in enger Zusammenarbeit mit dem ECTU-Team, unseren Prüfärzt*innen sowie externen Partnern und Sponsoren
TUM Klinikum Rechts der Isar * München * Befristeter Vertrag * Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Ihr Universitätsklinikum im Herzen Münchens - Wir sind das TUM Klinikum Rechts der Isar und verlässlicher Arbeitgeber für rund 6.600 Mitarbeiter*innen. Als Uniklinikum widmen wir uns neben der Krankenversorgung auch der Forschung und Lehre – entsprechend unserem Leitbild „Wissenschaft Heilung“ und genießen national wie international einen ausgezeichneten Ruf. 160 unterschiedliche Berufsgruppen arbeiten Hand in Hand, um unseren Patient*innen eine optimale Behandlung zukommen zu lassen. Voll- und Teilzeit | befristet (12 Monate) * Sie übernehmen die Koordination und die Begleitung von Vertragsverhandlungen in enger Zusammenarbeit mit dem ECTU-Team, unseren Prüfärzt*innen sowie externen Partnern und Sponsoren
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Chemikant / Biologe / Mediziner / Gesundheitswissenschaftler / Pharmazeut / MTA als Medical Approver (m/w/d)
Chemikant / Biologe / Mediziner / Gesundheitswissenschaftler / Pharmazeut / MTA als Medical Approver (m/w/d)
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG
Garmisch-Partenkirchen, Bad Homburg, München
Teilweise Home-Office
Schnelle Bewerbung
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG * Garmisch-Partenkirchen, Bad Homburg, München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Als Spezialisten im Healthcare Markt führen wir jährlich über 2.000 Veranstaltungen durch. Unser Portfolio deckt dabei sämtliche Bereiche aus Kreation, Administration und Vor-Ort-Organisation ab: Ideenfindung und Konzeption, Auswahl von Location und Referierenden, Management der Teilnehmenden, Nachhaltigkeitsberatung, CME-Zertifizierung, Einhaltung der Pharma-Compliance-Regeln, technische Ausstattung, Catering und vieles mehr. Starte jetzt bei uns durch. Wir geben dir die Möglichkeit, dich mit deinen Talenten in einem abwechslungsreichen Beruf mit Perspektive auszuleben – als Teil eines jungen, engagierten Teams.
HEALTHCARE CONVENTION a brand of Europe Convention GmbH & CO KG * Garmisch-Partenkirchen, Bad Homburg, München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Über uns - Als Spezialisten im Healthcare Markt führen wir jährlich über 2.000 Veranstaltungen durch. Unser Portfolio deckt dabei sämtliche Bereiche aus Kreation, Administration und Vor-Ort-Organisation ab: Ideenfindung und Konzeption, Auswahl von Location und Referierenden, Management der Teilnehmenden, Nachhaltigkeitsberatung, CME-Zertifizierung, Einhaltung der Pharma-Compliance-Regeln, technische Ausstattung, Catering und vieles mehr. Starte jetzt bei uns durch. Wir geben dir die Möglichkeit, dich mit deinen Talenten in einem abwechslungsreichen Beruf mit Perspektive auszuleben – als Teil eines jungen, engagierten Teams.
Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or sample metadata, and analysis outputs.
Manage and integrate multi-source datasets, including digital pathology images, sample metadata, clinical trial information, real-world data, and image analysis outputs. * Demonstrated experience transferring and handling multi-source and multimodal biomedical datasets, including imaging data, clinical trial data, patient or sample metadata, and analysis outputs.
Your work will ensure that pathology workflows and imaging data are executed, structured, and leveraged to accelerate discovery, improve clinical trial decision-making, and deliver validated diagnostic tools that advance patient care. The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * Define, implement and monitor end-to-end CP delivery workflows translating research, clinical, and diagnostic needs into practical execution, in collaboration with Quality Management and cross-functional teams, * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use * Collaborate with Regulatory, Quality, and Clinical Affairs to ensure traceability and compliance of all diagnostic-related datasets
Your work will ensure that pathology workflows and imaging data are executed, structured, and leveraged to accelerate discovery, improve clinical trial decision-making, and deliver validated diagnostic tools that advance patient care. The ideal candidate brings strong experience in digital pathology operations and data management, along with a practical understanding of clinical development and diagnostic requirements. * Define, implement and monitor end-to-end CP delivery workflows translating research, clinical, and diagnostic needs into practical execution, in collaboration with Quality Management and cross-functional teams, * Drive initiatives to make clinical pathology data analysis-ready for downstream discovery and regulatory use * Collaborate with Regulatory, Quality, and Clinical Affairs to ensure traceability and compliance of all diagnostic-related datasets
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Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions.
Ideals Virtual Data Room (VDR): Secure document sharing and collaboration for due diligence, fundraising, corporate reporting, licensing, clinical trials, and other complex transactions.
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Schnelle Bewerbung
Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
NEU
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Site Activation Manager (Contract Specialist - Germany - hybrid in München)
Site Activation Manager (Contract Specialist - Germany - hybrid in München)
Syneos Health Inc.
München
Excellent understanding of clinical trial process across Phases II-IV and ICH GCP - Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. For one of our sponsors we are currently recruiting for a contract specialist / financial clinical operations specialist to join the team. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. * Good understanding clinical protocols and associated study specifications.
Excellent understanding of clinical trial process across Phases II-IV and ICH GCP - Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. For one of our sponsors we are currently recruiting for a contract specialist / financial clinical operations specialist to join the team. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients. * Good understanding clinical protocols and associated study specifications.
NEU
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Schnelle Bewerbung
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 * 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 * 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
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Associate Director Country Operations Management
Associate Director Country Operations Management
Alexion Pharma Germany GmbH
Germany - Munich
Teilweise Home-Office
Schnelle Bewerbung
Contribute to Country feasibility analysis for new potential clinical trials (as applicable, depending on the direct reports the LM will be managing). The AD COM is accountable for all assigned operational trial deliverables across programs are completed according to timelines, operational procedures, quality standards, SOPs and guidelines, independently if the trial is directly manage by the AD COM or by his/her direct reports. Maintain tools to document and track clinical monitoring activities as required.
Contribute to Country feasibility analysis for new potential clinical trials (as applicable, depending on the direct reports the LM will be managing). The AD COM is accountable for all assigned operational trial deliverables across programs are completed according to timelines, operational procedures, quality standards, SOPs and guidelines, independently if the trial is directly manage by the AD COM or by his/her direct reports. Maintain tools to document and track clinical monitoring activities as required.
NEU
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. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the ...
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. * End to end electronic Trial Master File (eTMF) set-up and maintenance, regulatory document tracking, tracking of team training documentation, milestone management in the ...
Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
Some of the key tasks you will be involved with are:- Supporting in the preparation and execution of clinical trials - Procurement of study materials and office supplies
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Director Medical Affairs Medical Lead HIV (m/f/d)
Director Medical Affairs Medical Lead HIV (m/f/d)
Healthcare Society e.V.
Munich Prinzregentenplatz
Teilweise Home-Office
You will work closely with various cross-functional counterparts and teams in commercial (across brands), market access, clinical operations etc. to ensure a well-balanced portfolio approach to ViiV's national promotional and scientific meetings and materials, pricing and reimbursement operations as well as clinical studies.
You will work closely with various cross-functional counterparts and teams in commercial (across brands), market access, clinical operations etc. to ensure a well-balanced portfolio approach to ViiV's national promotional and scientific meetings and materials, pricing and reimbursement operations as well as clinical studies.
Schnelle Bewerbung
Development and implementation of the local medical strategy to support clinical practice and the objectives of the overall company. * Responsibility for the implementation of new medical practices, the evaluation of new indications, analysis of the status quo of current treatment and patient pathways, identification of patients for clinical research, and the development of a deep understanding of the respective indication area.
Development and implementation of the local medical strategy to support clinical practice and the objectives of the overall company. * Responsibility for the implementation of new medical practices, the evaluation of new indications, analysis of the status quo of current treatment and patient pathways, identification of patients for clinical research, and the development of a deep understanding of the respective indication area.
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Schnelle Bewerbung
Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply.
Our expertise also covers biologicals, orphan drugs, clinical trials, fill-and-finish, and lyophilization, offering end-to-end solutions from product development to commercial supply.
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