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134 Treffer für Clinical Research Jobs in Unterhaching im Umkreis von 30 km
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Clinician for the Clinical Centre of Excellence (f/m/d)
Clinician for the Clinical Centre of Excellence (f/m/d)
TÜV SÜD
München, Ahmedabad, Madrid, Lissabon, Warschau
Teilweise Home-Office
Assessing clinical evaluations as part of technical documentation assessments according to the requirements layed down in the European Medical Device Regulation (MDR) * Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support and close exchange with colleagues * Optionally providing support during audits of clinical processes of as a clinial expert (remote or on-site) * Four years of clinical practice in health care services or related sectors in the area of Cardiac surgery * Two years of experience in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices * Experience with MDR, regulatory aspects of medical devices, clinical evaluation for medical devices / medical writing is a plus.
Assessing clinical evaluations as part of technical documentation assessments according to the requirements layed down in the European Medical Device Regulation (MDR) * Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support and close exchange with colleagues * Optionally providing support during audits of clinical processes of as a clinial expert (remote or on-site) * Four years of clinical practice in health care services or related sectors in the area of Cardiac surgery * Two years of experience in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices * Experience with MDR, regulatory aspects of medical devices, clinical evaluation for medical devices / medical writing is a plus.
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Knowledge of clinical research, ICH GCP and local regulations - The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. * Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
Knowledge of clinical research, ICH GCP and local regulations - The Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials; as well as providing oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of Clinical Monitoring, CRAs, and Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. * Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues.
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Senior Clinical Research Associate (w/m/d) - sponsor dedicated - home based
Senior Clinical Research Associate (w/m/d) - sponsor dedicated - home based
Fortrea Germany GmbH
München
Teilweise Home-Office
alternativ eine abgeschlossene Berufsausbildung im Bereich Gesundheit / Pflege, oder gleichwertige Berufserfahrung in der klinischen Forschung (z. B. als Study Nurse, Research Nurse, Studienkoordinator*in...)
alternativ eine abgeschlossene Berufsausbildung im Bereich Gesundheit / Pflege, oder gleichwertige Berufserfahrung in der klinischen Forschung (z. B. als Study Nurse, Research Nurse, Studienkoordinator*in...)
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Randstad Deutschland GmbH & Co. KG * München - Firmenbeschreibung - Ihre Karriere ist kein Zufall! Profitieren Sie von unserem einzigartigen Netzwerk: Randstad professional solutions sucht aktuell im Raum München einen biologisch-technischen Assistenten. Sie sind Technical Assistant und auf der Suche nach einer neuen Herausforderung in der Pharmabranche? Vertrauen Sie unserer Expertise und nutzen Sie unser Sprungbrett zum Erfolg. Bewerben Sie sich jetzt direkt online! Wir legen Wert auf Chancengleichheit und begrüßen die Bewerbung von Menschen mit Behinderung, deren Inklusion uns ein besonderes Anliegen ist. Ihre Aufgaben * Unterstützung des bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support * Kontinuierliche Verwaltung und Archivierung von Studiendokumenten und deren Administration
Randstad Deutschland GmbH & Co. KG * München - Firmenbeschreibung - Ihre Karriere ist kein Zufall! Profitieren Sie von unserem einzigartigen Netzwerk: Randstad professional solutions sucht aktuell im Raum München einen biologisch-technischen Assistenten. Sie sind Technical Assistant und auf der Suche nach einer neuen Herausforderung in der Pharmabranche? Vertrauen Sie unserer Expertise und nutzen Sie unser Sprungbrett zum Erfolg. Bewerben Sie sich jetzt direkt online! Wir legen Wert auf Chancengleichheit und begrüßen die Bewerbung von Menschen mit Behinderung, deren Inklusion uns ein besonderes Anliegen ist. Ihre Aufgaben * Unterstützung des bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support * Kontinuierliche Verwaltung und Archivierung von Studiendokumenten und deren Administration
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Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (DZNE) * München * Befristeter Vertrag * Teilzeit - Das Deutsche Zentrum für Neurodegenerative Erkrankungen (DZNE) ist ein weltweit führendes, international ausgerichtetes Forschungszentrum, das sich der Entdeckung neuer Ansätze zur Prävention und Behandlung neurodegenerativer Erkrankungen verschrieben hat. Code: 2114/2026/4 - in Teilzeit, zunächst befristet auf zwei Jahre - Standort: München - Ihre Rolle im Detail * Studienvorbereitung und Studiendurchführung in Zusammenarbeit mit der Prüfgruppe * Planung, Organisation und Durchführung studienspezifischer Maßnahmen nach Prüfprotokoll * Patientenbetreuung * Ansprechpartner und Schnittstelle für , Monitor, Prüfgruppe und Patient * Erhebung und Dokumentation studienrelevanter Daten in Deutsch und Englisch * Aufbereitung, Versand und Dokumentation von gewonnenem Biomaterial
Deutsches Zentrum für Neurodegenerative Erkrankungen e.V. (DZNE) * München * Befristeter Vertrag * Teilzeit - Das Deutsche Zentrum für Neurodegenerative Erkrankungen (DZNE) ist ein weltweit führendes, international ausgerichtetes Forschungszentrum, das sich der Entdeckung neuer Ansätze zur Prävention und Behandlung neurodegenerativer Erkrankungen verschrieben hat. Code: 2114/2026/4 - in Teilzeit, zunächst befristet auf zwei Jahre - Standort: München - Ihre Rolle im Detail * Studienvorbereitung und Studiendurchführung in Zusammenarbeit mit der Prüfgruppe * Planung, Organisation und Durchführung studienspezifischer Maßnahmen nach Prüfprotokoll * Patientenbetreuung * Ansprechpartner und Schnittstelle für , Monitor, Prüfgruppe und Patient * Erhebung und Dokumentation studienrelevanter Daten in Deutsch und Englisch * Aufbereitung, Versand und Dokumentation von gewonnenem Biomaterial
The Senior Clinical Trial Coordinator assists the clinical research team to ensure that the study is conducted in accordance with GCP, all relevant SOPs, the protocol and in respect of the budget and timelines. * Previous experience in clinical research (in CROs, Pharma or academy/hospital experience) * Good knowledge of Clinical Research and Regulatory/Ethical requirements - They will oversee and mentor junior Clinical and as needed.
The Senior Clinical Trial Coordinator assists the clinical research team to ensure that the study is conducted in accordance with GCP, all relevant SOPs, the protocol and in respect of the budget and timelines. * Previous experience in clinical research (in CROs, Pharma or academy/hospital experience) * Good knowledge of Clinical Research and Regulatory/Ethical requirements - They will oversee and mentor junior Clinical and as needed.
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Schnelle Bewerbung
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 * Ability to consult with , interpret research requirements, and determine statistical analysis strategies
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 * Ability to consult with , interpret research requirements, and determine statistical analysis strategies
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Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards.
Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards.
NEU
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Schnelle Bewerbung
Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries. He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives. * Identify and implement appropriate high-impact medical research projects to support the business objectives, including Alexion–sponsored and investigator-initiated projects.
Identify potential investigators in relevant diseases for participation in future clinical research projects and disease registries. He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. * Support the development and drive implementation of a local Medical Affairs Plan and strategy, to support best clinical practice and the overall corporate objectives. * Identify and implement appropriate high-impact medical research projects to support the business objectives, including Alexion–sponsored and investigator-initiated projects.
The Study Start Up (SSU) Associate function is to support the with all SSU-related activities in collaboration with other clinical research stakeholders and to serve as a contact for local/global SSU process improvements. * Submission of the clinical study agreement for review, as needed. * Clinical Trial Health Authority application and regulatory submission process. * Provide continuous and proactive communication with ECs / hospital administration / industry bodies to obtain accurate and up to date information on clinical trial status and activities. * Prior work experience demonstrating knowledge and understanding of clinical trials. * Demonstrated knowledge and understanding of ICH-GCP and a desire to increase specialist knowledge in regulatory, ethics and contractual requirements for SSU in clinical trials for European and international trials.
The Study Start Up (SSU) Associate function is to support the with all SSU-related activities in collaboration with other clinical research stakeholders and to serve as a contact for local/global SSU process improvements. * Submission of the clinical study agreement for review, as needed. * Clinical Trial Health Authority application and regulatory submission process. * Provide continuous and proactive communication with ECs / hospital administration / industry bodies to obtain accurate and up to date information on clinical trial status and activities. * Prior work experience demonstrating knowledge and understanding of clinical trials. * Demonstrated knowledge and understanding of ICH-GCP and a desire to increase specialist knowledge in regulatory, ethics and contractual requirements for SSU in clinical trials for European and international trials.
Schnelle Bewerbung
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. * Development and implementation of the local medical strategy to support clinical practice and the objectives of the overall company.
Schnelle Bewerbung
The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements. The CSM works in close collaboration with Study Start-Up (SSU) manager, Clinical Study Administrator (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. The CSM is responsible for ensuring that all requirements for site activation are in place for the agreed number of centers in clinical studies according to SOPs. * Reviewing Clinical Monitoring Documentation (reports, metrics, etc) for the assigned studies. * Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP).
The Country Study Manager (CSM) has local responsibility for the delivery of the studies in compliance with Good Clinical Practice (GCP), and regulatory requirements. The CSM works in close collaboration with Study Start-Up (SSU) manager, Clinical Study Administrator (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. The CSM is responsible for ensuring that all requirements for site activation are in place for the agreed number of centers in clinical studies according to SOPs. * Reviewing Clinical Monitoring Documentation (reports, metrics, etc) for the assigned studies. * Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP).
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Schnelle Bewerbung
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. 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
Since our founding in 1997, we have been awarded three times as the best service provider and the best contract research organization internationally. 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
The Vice President, Monitoring and Site Engagement is a key member of the Alira Health Clinical leadership team. In this role, the VP oversees the Directors of Clinical Monitoring in Europe and North America, ensuring operational excellence across all monitoring activities and the consistent delivery of high‑quality outcomes to sponsors while meeting expectations, timelines, and regulatory standards. * Serves as a leader, point of mentorship, and point of escalation for the DirectorsDirectors of Clinical Monitoring, and Director(s) of Study Start Up. * Develops and maintains, together with the local Alira Health teams and local CRO partners as applicable, a network of existing and potential clinical study sites across all regions, and facilitates partnership with institutions to build a framework of collaboration.
The Vice President, Monitoring and Site Engagement is a key member of the Alira Health Clinical leadership team. In this role, the VP oversees the Directors of Clinical Monitoring in Europe and North America, ensuring operational excellence across all monitoring activities and the consistent delivery of high‑quality outcomes to sponsors while meeting expectations, timelines, and regulatory standards. * Serves as a leader, point of mentorship, and point of escalation for the DirectorsDirectors of Clinical Monitoring, and Director(s) of Study Start Up. * Develops and maintains, together with the local Alira Health teams and local CRO partners as applicable, a network of existing and potential clinical study sites across all regions, and facilitates partnership with institutions to build a framework of collaboration.
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Head of Medical Safety GCSP (m/f/d)
Head of Medical Safety GCSP (m/f/d)
Bavarian Nordic GmbH
Martinsried bei München, Bern
Teilweise Home-Office
We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe (e.g., Martinsried, Germany) and North America. We are looking for an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP). As our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. * Ensure high-quality clinical safety contributions to development programs and for the life-cycle management of marketed products in compliance with regulations, guidelines, BN operating procedures (SOPs) To succeed in this role, you must have a medical doctorate (MD) and leadership experience in clinical safety and pharmacovigilance.
We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe (e.g., Martinsried, Germany) and North America. We are looking for an experienced Head of Medical Safety GCSP providing medical leadership across Global Clinical Safety & Pharmacovigilance (GCSP). As our Head of Medical Safety GCSP, you will be accountable for all medical safety related aspects of clinical safety and pharmacovigilance as well as ad hoc safety issues and innovation projects in your area of expertise. * Ensure high-quality clinical safety contributions to development programs and for the life-cycle management of marketed products in compliance with regulations, guidelines, BN operating procedures (SOPs) To succeed in this role, you must have a medical doctorate (MD) and leadership experience in clinical safety and pharmacovigilance.
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Our light, electron and X-ray microscopes as well as software solutions that utilize AI technology enable groundbreaking discoveries in life science, materials and industrial research as well as for education and clinical practice. ZEISS Research Microscopy Solutions is a world leader in the manufacture of microscopy systems for the visualization of the tiniest structures and particles in the fields of research and science. Renowned scientists rely on ZEISS microscopes for their research, including Robert Koch, who discovered the tuberculosis pathogen around 1900.
Our light, electron and X-ray microscopes as well as software solutions that utilize AI technology enable groundbreaking discoveries in life science, materials and industrial research as well as for education and clinical practice. ZEISS Research Microscopy Solutions is a world leader in the manufacture of microscopy systems for the visualization of the tiniest structures and particles in the fields of research and science. Renowned scientists rely on ZEISS microscopes for their research, including Robert Koch, who discovered the tuberculosis pathogen around 1900.
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
Schnelle Bewerbung
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
Conceptualize and coordinate engagement of PAOs in clinical development programs running and/or planned in Germany * Most importantly, a passion for patients and research
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Schnelle Bewerbung
We support organizations in implementing digital innovations — Virtual, Augmented, and Mixed Reality as well as AI — particularly for learning, training, and real-time assistance in clinical and care environments. ARAIAS introduces a new approach to hands-on, safe, and evidence-based learning and training in clinical settings, with the long-term goal of reducing workload for and improving care outcomes. The near-term focus is on validating the AI models, establishing the core technical foundations, and building toward a proof of concept we can test in real education and clinical settings. * Meaningful work — You help shape how technology redefines education and training in healthcare, with real impact on clinical outcomes * International collaboration — Work alongside a Taiwan-based partner covering technology, hardware, and research
We support organizations in implementing digital innovations — Virtual, Augmented, and Mixed Reality as well as AI — particularly for learning, training, and real-time assistance in clinical and care environments. ARAIAS introduces a new approach to hands-on, safe, and evidence-based learning and training in clinical settings, with the long-term goal of reducing workload for and improving care outcomes. The near-term focus is on validating the AI models, establishing the core technical foundations, and building toward a proof of concept we can test in real education and clinical settings. * Meaningful work — You help shape how technology redefines education and training in healthcare, with real impact on clinical outcomes * International collaboration — Work alongside a Taiwan-based partner covering technology, hardware, and research
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Research Scientist (m/f/d) in Social Sciences and / or Engineering in the Field of Passenger Demand and Trend Analysis in Aviation
Research Scientist (m/f/d) in Social Sciences and / or Engineering in the Field of Passenger Demand and Trend Analysis in Aviation
Bauhaus Luftfahrt e.V.
Taufkirchen bei München
Teilweise Home-Office
Research Scientist (m/f/d) in Social Sciences and / or Engineering * Acknowledged research institution – with our feet on the ground and our thoughts in the air
Research Scientist (m/f/d) in Social Sciences and / or Engineering * Acknowledged research institution – with our feet on the ground and our thoughts in the air
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Wir suchen ab 1. August 2026 einen Werkstudenten (m/w/d) im Bereich Research & Library - In der Research- & Library-Abteilung einer internationalen Großkanzlei tauchen Sie tief in die spannende Welt des Wissensmanagements ein.
Wir suchen ab 1. August 2026 einen Werkstudenten (m/w/d) im Bereich Research & Library - In der Research- & Library-Abteilung einer internationalen Großkanzlei tauchen Sie tief in die spannende Welt des Wissensmanagements ein.
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Schnelle Bewerbung
Roland Berger Holding GmbH & Co. KGaA * München * Studentenjobs, Werkstudent * Teilzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Roland Berger ist eine der weltweit führenden Strategieberatungen mit einem breiten Serviceportfolio für alle relevanten Branchen und Geschäftsfunktionen. Wir schätzen unterschiedliche Perspektiven und Ansätze und setzen auf die Vielfalt und Authentizität unserer Mitarbeitenden. Getrieben von unseren Werten Unternehmertum, Exzellenz und Empathie, sind wir bei Roland Berger überzeugt, dass wir ein neues, nachhaltiges Paradigma benötigen, das den gesamten Wertschöpfungszyklus berücksichtigt. Unsere interdisziplinären Teams arbeiten mit unseren Kunden zusammen, um die Herausforderungen unserer Zeit erfolgreich anzugehen – heute und morgen, in allen Branchen und Geschäftsfunktionen.
Roland Berger Holding GmbH & Co. KGaA * München * Studentenjobs, Werkstudent * Teilzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Roland Berger ist eine der weltweit führenden Strategieberatungen mit einem breiten Serviceportfolio für alle relevanten Branchen und Geschäftsfunktionen. Wir schätzen unterschiedliche Perspektiven und Ansätze und setzen auf die Vielfalt und Authentizität unserer Mitarbeitenden. Getrieben von unseren Werten Unternehmertum, Exzellenz und Empathie, sind wir bei Roland Berger überzeugt, dass wir ein neues, nachhaltiges Paradigma benötigen, das den gesamten Wertschöpfungszyklus berücksichtigt. Unsere interdisziplinären Teams arbeiten mit unseren Kunden zusammen, um die Herausforderungen unserer Zeit erfolgreich anzugehen – heute und morgen, in allen Branchen und Geschäftsfunktionen.
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Wir suchen zum nächstmöglichen Termin in München einen Market Research Manager (m/w/d)
Wir suchen zum nächstmöglichen Termin in München einen Market Research Manager (m/w/d)
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Schnelle Bewerbung
HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. The successful candidate should not only understand clinical pharmacology, DMPK, PopPK, PBPK, PK/PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. The role requires someone who has worked in or closely with the pharmaceutical industry and understands how development decisions are made under real-world constraints of time, budget, regulatory risk, and clinical feasibility. • Lead HMNC's clinical pharmacology and DMPK strategy across pipeline programs, ensuring alignment with clinical ...
HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. The successful candidate should not only understand clinical pharmacology, DMPK, PopPK, PBPK, PK/PD, ADME, and safety data, but also be able to interpret these data critically and translate them into clear development decisions. The role requires someone who has worked in or closely with the pharmaceutical industry and understands how development decisions are made under real-world constraints of time, budget, regulatory risk, and clinical feasibility. • Lead HMNC's clinical pharmacology and DMPK strategy across pipeline programs, ensuring alignment with clinical ...
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Lead Research Engineer (f/m/d): Foundation and World Models on Structured Data
Lead Research Engineer (f/m/d): Foundation and World Models on Structured Data
SAP SE
Garching bei München, DE, 85748
At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and models, with the goal to publish benchmarks and models at scientific conferences and in the open-source community. Define and drive open source model and software contributions based on research deliverables. Knowledge of latest research and development trends in Foundation Models on Structured Data.
At SAP's Business AI Research, we are exploring the next frontier of AI methods on structured business data – graphs, tables, time series, and more. We collaborate with our existing applied research teams in creating novel benchmarks for business problems and the development of novel architectures and models, with the goal to publish benchmarks and models at scientific conferences and in the open-source community. Define and drive open source model and software contributions based on research deliverables. Knowledge of latest research and development trends in Foundation Models on Structured Data.
Beliebte Jobs
- Physiotherapeut Ausbildung
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- Einkauf
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- Vertrieb und Verkauf
- Logopädie Ausbildung
- Kommunikation
- Pflegehelfer Ausbildung
- Arzt Ausbildung
- Rettungssanitäter Ausbildung
- Kfz Mechaniker Ausbildung
- Heilpraktiker Ausbildung
- MFA Ausbildung
- English Speaking
- Ausbildung Bauzeichner
- Polizei Ausbildung