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31 Treffer für Clinical Trial Jobs in Planegg im Umkreis von 30 km
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Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)
Associate Director (m/f/d), Computational Pathology Biomarker Lead (Oncology/BioPharma)
AstraZeneca
München
Understanding of biomarker development pathways, clinical trial design, and translational research strategies across different stages of drug development. Do you thrive at the intersection of AI innovation and clinical translation? In this position you will work with a multi-disciplinary team to pioneer AI-enabled computational pathology and multi-modal biomarkers that fundamentally change how we approach patient selection and drug development, aiming to improve clinical outcomes. Within AI for Computational Pathology and Biomarkers, we're pioneering AI-powered solutions that transform patient selection, biomarker development, and clinical decision-making at enterprise scale. * Provide scientific leadership for AI-powered computational pathology and multimodal biomarker development across AstraZeneca's Oncology and/or BioPharmaceuticals portfolio, delivering biomarkers that ...
Understanding of biomarker development pathways, clinical trial design, and translational research strategies across different stages of drug development. Do you thrive at the intersection of AI innovation and clinical translation? In this position you will work with a multi-disciplinary team to pioneer AI-enabled computational pathology and multi-modal biomarkers that fundamentally change how we approach patient selection and drug development, aiming to improve clinical outcomes. Within AI for Computational Pathology and Biomarkers, we're pioneering AI-powered solutions that transform patient selection, biomarker development, and clinical decision-making at enterprise scale. * Provide scientific leadership for AI-powered computational pathology and multimodal biomarker development across AstraZeneca's Oncology and/or BioPharmaceuticals portfolio, delivering biomarkers that ...
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Senior Scientist Drug Product Process Development (gn) 2-Year Fixed-Term Contract
Senior Scientist Drug Product Process Development (gn) 2-Year Fixed-Term Contract
Formycon AG
Planegg
Teilweise Home-Office
With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
With an experienced team comprised of around 200 highly skilled professionals, the company is able to span the entire value chain of biosimilar drug development, from market analysis and target definition by protein analytics, to the development of production processes, to clinical trials and the regulatory approval process.
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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. They will oversee and mentor junior Clinical and as needed. * Previous experience in clinical research (in CROs, Pharma or academy/hospital experience) * Good knowledge of Clinical Research and Regulatory/Ethical requirements
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. They will oversee and mentor junior Clinical and as needed. * Previous experience in clinical research (in CROs, Pharma or academy/hospital experience) * Good knowledge of Clinical Research and Regulatory/Ethical requirements
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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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Unterstützung des bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support
Unterstützung des bzw. des Contracting-Teams im Bereich der klinischen Forschung als Trial Support
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. * Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS). * Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture - The Sr CRA is an important member of the Alira Health Clinical team. 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 ...
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. * Coordinates with appropriate cross-functional departments to facilitate negotiation/issue resolution for clinical trial monitoring related issues. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS). * Good computer skills, with ability to use clinical trial management systems, clinical trial databases and electronic data capture - The Sr CRA is an important member of the Alira Health Clinical team. 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 ...
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. 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.
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Schnelle Bewerbung
Proven experience in the oversight and delivery of operational aspects of all stages of of clinical trial process. 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. * Leading recruitment discussions at local level for the assigned trials. * Coordination of study specific training of CRAs for assigned trials.
Proven experience in the oversight and delivery of operational aspects of all stages of of clinical trial process. 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. * Leading recruitment discussions at local level for the assigned trials. * Coordination of study specific training of CRAs for assigned trials.
Experience in monitoring all phases of clinical trials required - 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.
Experience in monitoring all phases of clinical trials required - 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.
NEU
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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
Fortrea Germany GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Als führendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft für wissenschaftliche Präzision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an Lösungen für die klinische Entwicklung, den Patientenzugang und die Technologie in mehr als 20 Therapiebereichen. Mit über 19.000 Mitarbeitern, in mehr als 90 Ländern, verändert Fortrea die Arzneimittel- und Medizinprodukteentwicklung für Partner und Patienten auf der ganzen Welt. Als Senior - CRA in unserer Abteilung Flexible Solutions sind Sie von zentraler Bedeutung für die erfolgreiche Durchführung komplexer klinischer Studien (Phasen I - III) in Deutschland.
Fortrea Germany GmbH * München * Feste Anstellung * Homeoffice möglich, Vollzeit - Sei einer der ersten Bewerber - Als führendes globales Auftragsforschungsinstitut (CRO) mit einer Leidenschaft für wissenschaftliche Präzision und einer jahrzehntelangen Erfahrung in der klinischen Entwicklung, bietet Fortrea Kunden aus der Pharma-, Biotechnologie- und Medizintechnikbranche ein breites Spektrum an Lösungen für die klinische Entwicklung, den Patientenzugang und die Technologie in mehr als 20 Therapiebereichen. Mit über 19.000 Mitarbeitern, in mehr als 90 Ländern, verändert Fortrea die Arzneimittel- und Medizinprodukteentwicklung für Partner und Patienten auf der ganzen Welt. Als Senior - CRA in unserer Abteilung Flexible Solutions sind Sie von zentraler Bedeutung für die erfolgreiche Durchführung komplexer klinischer Studien (Phasen I - III) in Deutschland.
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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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.
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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
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.
Noch nichts dabei? Es gibt 16 weitere Jobs, die zu deiner Suche passen könnten
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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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Act as a clinical and product expert, training and supporting and sales teams in the application of arthroplasty solutions * Plan and conduct practical training sessions (e.g. cadaver labs, workshops, and product demonstrations) with a strong focus on clinical excellence * Strong clinical background (e.g. medicine, biomedical sciences) or alternatively a commercial background combined with solid experience in arthroplasty (Hip & Knee) * Experience in a customer-facing role (e.g. sales, application specialist, clinical support) with a strong focus on relationship building * Strong communication and presentation skills, paired with a high level of credibility in clinical environments
Act as a clinical and product expert, training and supporting and sales teams in the application of arthroplasty solutions * Plan and conduct practical training sessions (e.g. cadaver labs, workshops, and product demonstrations) with a strong focus on clinical excellence * Strong clinical background (e.g. medicine, biomedical sciences) or alternatively a commercial background combined with solid experience in arthroplasty (Hip & Knee) * Experience in a customer-facing role (e.g. sales, application specialist, clinical support) with a strong focus on relationship building * Strong communication and presentation skills, paired with a high level of credibility in clinical environments
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Senior Regulatory Affairs Specialist (m/f/d)
Senior Regulatory Affairs Specialist (m/f/d)
Dornier MedTech Systems GmbH
Weßling
Teilweise Home-Office
Schnelle Bewerbung
Support Clinical Evaluation, Vigilance / Post-Marketing Surveillance activities
Support Clinical Evaluation, Vigilance / Post-Marketing Surveillance activities
NEU
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Develop relationships with HCPs and clinical sites to support effective product evaluations, case studies, and long-term adoption. * Act as trusted scientific expert, delivering accurate and compliant medical science and clinical education to external stakeholders. * Deliver tailored educational programs to HCPs, ensuring dissemination of our latest scientific and clinical evidence. * Collaborate with established and emerging KOLs on clinical evidence generation to validate our products. * Proactively engage KOL networks to gather insights, inform clinical practice, and support the adoption of our innovative solutions. * Collect product performance and user feedback for Research & Development (R&D), Medical & Clinical Affairs (MACA), and commercial teams to inform life cycle management, next-generation innovations, clinical study designs, and commercial strategies.
Develop relationships with HCPs and clinical sites to support effective product evaluations, case studies, and long-term adoption. * Act as trusted scientific expert, delivering accurate and compliant medical science and clinical education to external stakeholders. * Deliver tailored educational programs to HCPs, ensuring dissemination of our latest scientific and clinical evidence. * Collaborate with established and emerging KOLs on clinical evidence generation to validate our products. * Proactively engage KOL networks to gather insights, inform clinical practice, and support the adoption of our innovative solutions. * Collect product performance and user feedback for Research & Development (R&D), Medical & Clinical Affairs (MACA), and commercial teams to inform life cycle management, next-generation innovations, clinical study designs, and commercial strategies.
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Schnelle Bewerbung
Plan and execute digital campaigns across Google Ads, Meta, and LinkedIn — targeting surgeons, residents, and clinical decision-makers * Direct exposure to the medtech world: clinical content, surgical audiences, global congresses
Plan and execute digital campaigns across Google Ads, Meta, and LinkedIn — targeting surgeons, residents, and clinical decision-makers * Direct exposure to the medtech world: clinical content, surgical audiences, global congresses
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Schnelle Bewerbung
Test bench trials and validations are part of your responsibilities, allowing you to contribute to the continuous improvement of our processes
Test bench trials and validations are part of your responsibilities, allowing you to contribute to the continuous improvement of our processes
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Domain-naher QA-Experte - Life Sciences (m/w/d)
Domain-naher QA-Experte - Life Sciences (m/w/d)
SPIRIT-TESTING Software & Services GmbH
München
Teilweise Home-Office
Clinical Operations
Clinical Operations
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Schnelle Bewerbung
Organize and prepare pilot trials, including coordination with internal teams * Participate to on-site pilot trials at external manufacturing facilities
Organize and prepare pilot trials, including coordination with internal teams * Participate to on-site pilot trials at external manufacturing facilities
Schnelle Bewerbung
Aktive Betreuung: Telefonische und schriftliche Kontaktaufnahme mit warmen Inbound-Leads, Trial-Nutzern und Bestandskunden (keine Kaltakquise).
Aktive Betreuung: Telefonische und schriftliche Kontaktaufnahme mit warmen Inbound-Leads, Trial-Nutzern und Bestandskunden (keine Kaltakquise).
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Sales Einstieg: B2B Sales / Business Development (m/w/d) | Legal Tech (Werkstudent)
Sales Einstieg: B2B Sales / Business Development (m/w/d) | Legal Tech (Werkstudent)
Silvernova Gmbh
Munich
Schnelle Bewerbung
Aktive Betreuung: Telefonische und schriftliche Kontaktaufnahme mit warmen Inbound-Leads, Trial-Nutzern und Bestandskunden (keine Kaltakquise).
Aktive Betreuung: Telefonische und schriftliche Kontaktaufnahme mit warmen Inbound-Leads, Trial-Nutzern und Bestandskunden (keine Kaltakquise).