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- Healthcare Management
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1 Treffer für Clinical Affairs Jobs in Landshut im Umkreis von 30 km
Noch nichts dabei? Es gibt 1 weiteren Job, der zu deiner Suche passen könnte
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Global Sales Manager (m/w/d) – IVF & Biotech
Global Sales Manager (m/w/d) – IVF & Biotech
Minitüb GmbH
Tiefenbach bei Landshut
Teilweise Home-Office
Enge Zusammenarbeit mit Produktmanagement, Marketing und Regulatory Affairs
Enge Zusammenarbeit mit Produktmanagement, Marketing und Regulatory Affairs
24 passende Jobs liegen außerhalb deiner Region
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Expert (m/w/d) Logistic Operations Distribution - Clinical Supply Planning & Operations
Expert (m/w/d) Logistic Operations Distribution - Clinical Supply Planning & Operations
Daiichi Sankyo Europe GmbH
Pfaffenhofen an der Ilm
Im Bereich Clinical Supply Planning & Operations übernehmen Sie eine zentrale Rolle in der globalen Distribution klinischer Prüfpräparate. * Enge Zusammenarbeit innerhalb der Global Clinical Supply Operation (Japan, USA, EU)
Im Bereich Clinical Supply Planning & Operations übernehmen Sie eine zentrale Rolle in der globalen Distribution klinischer Prüfpräparate. * Enge Zusammenarbeit innerhalb der Global Clinical Supply Operation (Japan, USA, EU)
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Wir suchen zum nächstmöglichen Zeitpunkt einen Manager Political Affairs (w/m/d)
Wir suchen zum nächstmöglichen Zeitpunkt einen Manager Political Affairs (w/m/d)
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Produktmanager (m/w/d)
Produktmanager (m/w/d)
CGM Clinical Europe GmbH
St. Wolfgang, Erlangen, Idstein, Berlin, Hamburg, Koblenz
Teilweise Home-Office
CGM Clinical Europe GmbH
CGM Clinical Europe GmbH
Technical Writer (m/w/d)
Technical Writer (m/w/d)
CGM Clinical Europe GmbH
St. Wolfgang, Erlangen, Idstein, Hamburg, Koblenz
Teilweise Home-Office
CGM Clinical Europe GmbH
CGM Clinical Europe GmbH
Manage and conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt.
Manage and conduct scouting activities and recommend CDMOs for clinical and launch site selection from Tech Mgmt.
Im Bereich Clinical Supply Planning & Operations übernehmen Sie eine zentrale Rolle in der globalen Distribution klinischer Prüfpräparate.
Im Bereich Clinical Supply Planning & Operations übernehmen Sie eine zentrale Rolle in der globalen Distribution klinischer Prüfpräparate.
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Clinical Application Specialist – Neurorehabilitation (m/w/d)
Clinical Application Specialist – Neurorehabilitation (m/w/d)
EGZOTECH SP Z O O
Region Süddeutschland
Teilweise Home-Office
Clinical Application Specialist – Neurorehabilitation * Klare Entwicklungs- und Karrieremöglichkeiten, z. B. Richtung Clinical Lead, Produkttrainer
Clinical Application Specialist – Neurorehabilitation * Klare Entwicklungs- und Karrieremöglichkeiten, z. B. Richtung Clinical Lead, Produkttrainer
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
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Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
AstraZeneca
bundesweit
Teilweise Home-Office
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
Wir suchen in einer Festanstellung eine/n Clinical Research Associate (CRA) (m/w/d) - Zelltherapie (Außendienst)
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Clinical Support Specialist STIWELL Deutschland (m/w/d)
Clinical Support Specialist STIWELL Deutschland (m/w/d)
MED-EL Medical Electronics
Deutschland, Home Office
als klinische/n Außendienstmitarbeiter*in „Clinical Support Specialist STIWELL Neurorehabilitation“ für Funktionelle Elektrostimulation (FES) in Vollzeit.
als klinische/n Außendienstmitarbeiter*in „Clinical Support Specialist STIWELL Neurorehabilitation“ für Funktionelle Elektrostimulation (FES) in Vollzeit.
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In this client-facing consulting role, you will take full responsibility for the setup and operational management of clinical trials on behalf of our clients in the pharmaceutical and medical device (including IVD) sectors. o Clinical budget negotiation and vendor contracting on behalf of the sponsor - o Clinical trial risk assessment - o Preparation and submission of Clinical Trial Applications (CTA) and management of deficiency communications - o Establishment and maintenance of clinical trial communication structures * Preparation and quality control of clinical trial documentation as required * 6+ years of hands-on experience in managing pharmaceutical clinical trials, complemented by solid experience in medical device studies. * Proven track reco
In this client-facing consulting role, you will take full responsibility for the setup and operational management of clinical trials on behalf of our clients in the pharmaceutical and medical device (including IVD) sectors. o Clinical budget negotiation and vendor contracting on behalf of the sponsor - o Clinical trial risk assessment - o Preparation and submission of Clinical Trial Applications (CTA) and management of deficiency communications - o Establishment and maintenance of clinical trial communication structures * Preparation and quality control of clinical trial documentation as required * 6+ years of hands-on experience in managing pharmaceutical clinical trials, complemented by solid experience in medical device studies. * Proven track reco
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Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) * Schnittstelle zu Quality & Regulatory Affairs zur Berücksichtigung regulatorischer Anforderungen (z. B. MDR, ISO 13485) im Projektkontext
Koordination internationaler, interdisziplinärer Projektteams (Software, Hardware, Data/AI, Clinical, Quality) * Schnittstelle zu Quality & Regulatory Affairs zur Berücksichtigung regulatorischer Anforderungen (z. B. MDR, ISO 13485) im Projektkontext
Cell Therapy Territory Operations Manager / Regional Cell Therapy Operations Lead (m/f/d)
Cell Therapy Territory Operations Manager / Regional Cell Therapy Operations Lead (m/f/d)
AstraZeneca
bundesweit
It delivers operational and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation. * Drive initiatives across clinical and commercial cell therapy from development through post-market. * Partner with internal teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing).
It delivers operational and clinical guidance for trials and commercial products, leads site activation, and provides ongoing operational, quality, and clinical oversight post-activation. * Drive initiatives across clinical and commercial cell therapy from development through post-market. * Partner with internal teams (Program Management, QA, Manufacturing, Supply Chain, Medical Affairs, Market Access, Compliance, Sales/Marketing).
This role is part of the Oncology R&D team tasked with supporting Clinical and Commercial production across multiple sites. * Collaborate across functions with Clinical Operations, Supply Chain, Medical, IT, and Commercial teams to meet the needs of patients and healthcare providers. * A collaborative spirit and the ability to work effectively across diverse teams including Clinical Ops, Supply Chain, Medical, and IT. * Exposure to process improvement, training, or SOP development in clinical or operational settings.
This role is part of the Oncology R&D team tasked with supporting Clinical and Commercial production across multiple sites. * Collaborate across functions with Clinical Operations, Supply Chain, Medical, IT, and Commercial teams to meet the needs of patients and healthcare providers. * A collaborative spirit and the ability to work effectively across diverse teams including Clinical Ops, Supply Chain, Medical, and IT. * Exposure to process improvement, training, or SOP development in clinical or operational settings.
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Lead a cross-functional squad of CRM, Product, Copywriting, and Clinical experts - ensuring tight alignment and high-velocity execution.
Lead a cross-functional squad of CRM, Product, Copywriting, and Clinical experts - ensuring tight alignment and high-velocity execution.
Collaborate with design, clinical, engineering, and analytics partners to turn evidence into action.
Collaborate with design, clinical, engineering, and analytics partners to turn evidence into action.
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Clinical Scientist (m/w/d)
Clinical Scientist (m/w/d)
Grifols Deutschland GmbH
Niederrad, 60 Frankfurt am Main-Frankfurt-Süd, Deutschland
Die Stelle ist dem Clinical Development Team * Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
Die Stelle ist dem Clinical Development Team * Beitrag zu regulatorischen Dokumenten wie Investigator Brochures, Pediatric Plans, Briefing Books, Clinical Study Reports, etc. * Mindestens 2 Jahre Erfahrung als Clinical Trial Scientist oder 5 Jahre als Clinical Program Leader (oder vergleichbare Position)
Collaborate cross-functionally with product, clinical, and engineering teams to align on strategy and user needs.
Collaborate cross-functionally with product, clinical, and engineering teams to align on strategy and user needs.
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Senior Specialist Fill / Finish Process
Senior Specialist Fill / Finish Process
West Pharmaceutical Services Deutschland GmbH & Co. KG
Home-Office
Teilweise Home-Office
Capability to work well in a matrix environment with R&D, QA, Legal, Regulatory Affairs, Product Management, Technical Customer Support, Sales, Marketing, Product Technology Service, and Global Communications
Capability to work well in a matrix environment with R&D, QA, Legal, Regulatory Affairs, Product Management, Technical Customer Support, Sales, Marketing, Product Technology Service, and Global Communications
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You will provide strategic to Regulatory Affairs, Quality Assurance, and Commercial leadership as well as provide support to other Avantor to mitigate legal risks.
You will provide strategic to Regulatory Affairs, Quality Assurance, and Commercial leadership as well as provide support to other Avantor to mitigate legal risks.
The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) * Understands clinical trial processes with a thorough knowledge of ICH a
The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs. * Performs monitoring activities related to selection, initiation, conduct (recruitment, quality data collection) and timely completion of oncology/hematology clinical trials within the assigned region. * Establish regular lines of communication with sites and reports site progress, issues and proposed action to Clinical Operations * Collaborates with Regional and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.) * Understands clinical trial processes with a thorough knowledge of ICH a
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Senior Manager / Associate Director Corporate Affairs, Germany (Government Affairs and Patient Advocacy)
Senior Manager / Associate Director Corporate Affairs, Germany (Government Affairs and Patient Advocacy)
BeiGene Germany GmbH
Germany Remote
Work closely with internal departments, including Clinical, Regulatory, Medical, Market Access, Legal, and Commercial teams, to align government affairs and patient advocacy strategies with business objectives. The Senior Manager/ Associate Director, Corporate Affairs, focusing on Government Affairs and Patient Advocacy, will play a crucial role in advancing the company's public policy objectives, fostering relationships with key stakeholders, and advocating for policies that support patient access to our therapies. * Helps develop and implement government affairs strategies to influence healthcare policy in alignment with the company's objectives. * Coordinate with global corporate affairs teams to ensure a consistent approach to government affairs a
Work closely with internal departments, including Clinical, Regulatory, Medical, Market Access, Legal, and Commercial teams, to align government affairs and patient advocacy strategies with business objectives. The Senior Manager/ Associate Director, Corporate Affairs, focusing on Government Affairs and Patient Advocacy, will play a crucial role in advancing the company's public policy objectives, fostering relationships with key stakeholders, and advocating for policies that support patient access to our therapies. * Helps develop and implement government affairs strategies to influence healthcare policy in alignment with the company's objectives. * Coordinate with global corporate affairs teams to ensure a consistent approach to government affairs a
Beliebte Jobs
- Healthcare Management
- Medizinischer Dienst
- Medizinische Verwaltung
- Regulatory Affairs
- Arztpraxen
- Praxismanagement
- Clinical Specialist
- Government Affairs
- Klinische Forschung
- Medizinische Sekretaerin
- Medical advisor
- Nurse
- Medical Affairs
- Mitarbeiter/in Regulatory Affairs
- Community Health Nurse
- Medical Information