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- Kassel
- Bochum
- Heidelberg
- Trier
- Siegen
- Aalen
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- Biberach an der Riß
- Bietigheim-Bissingen
- Homburg
- Wien
- Spaichingen
- Ohrdruf
- Europa
- Westliches Europa
- Westdeutschland
- Süddeutschland
- Nordrhein-Westfalen
- Norddeutschland
- Südwestdeutschland
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- Rhein-Main-Gebiet
- Südbayern
- Niederrhein
- Taunus
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129 Treffer für Clinical Trial Assistant Jobs
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As a Technical Assistant (TA) (m/f/d) based in Martinsried, you will play a key role in advancing our proteomics workflows by supporting both innovation and research activities. * M.Sc. in a scientific field or at least 2 years of experience as a technical assistant
As a Technical Assistant (TA) (m/f/d) based in Martinsried, you will play a key role in advancing our proteomics workflows by supporting both innovation and research activities. * M.Sc. in a scientific field or at least 2 years of experience as a technical assistant
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Schnelle Bewerbung
CarboCode Germany GmbH * Konstanz * Feste Anstellung * Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Human natural lipid and oligosaccharide molecule-based food and health care products despite of being at high customer demand are currently not available at the market due to the complexity of their synthesis. CarboCode is a company that aspiring to improve human health and wellbeing by making human natural lipid and oligosaccharide molecules widely available. CarboCode core capabilities spans a variety of technologies spanning through advanced chemical synthesis, to biocatalysis and biotechnological production. This exciting position is a great opportunity for you to work for a of a wide range of innovative human care and food products, supporting world-class R&D, pilot-scale manufacturing and commercial operations. Your tasks
CarboCode Germany GmbH * Konstanz * Feste Anstellung * Vollzeit - Sei einer der ersten Bewerber - Schnelle Bewerbung - Human natural lipid and oligosaccharide molecule-based food and health care products despite of being at high customer demand are currently not available at the market due to the complexity of their synthesis. CarboCode is a company that aspiring to improve human health and wellbeing by making human natural lipid and oligosaccharide molecules widely available. CarboCode core capabilities spans a variety of technologies spanning through advanced chemical synthesis, to biocatalysis and biotechnological production. This exciting position is a great opportunity for you to work for a of a wide range of innovative human care and food products, supporting world-class R&D, pilot-scale manufacturing and commercial operations. Your tasks
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KERRY GROUP SERVICES LIMITED * Leipzig * Feste Anstellung * Vollzeit - Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. Your tasks - Are you a hands-on scientist who thrives at the intersection of research excellence and laboratory leadership? Do you enjoy building something new, shaping robust scientific operations, and seeing your work translate into real-world health impact?
KERRY GROUP SERVICES LIMITED * Leipzig * Feste Anstellung * Vollzeit - Kerry is the world's leading taste and nutrition company for the food, beverage and pharmaceutical industries. Every day we partner with customers to create healthier, tastier and more sustainable products that are consumed by billions of people across the world. Our vision is to be our customers' most valued partner, creating a world of sustainable nutrition. A career with Kerry offers you an opportunity to shape the future of food while providing you opportunities to explore and grow in a truly global environment. Your tasks - Are you a hands-on scientist who thrives at the intersection of research excellence and laboratory leadership? Do you enjoy building something new, shaping robust scientific operations, and seeing your work translate into real-world health impact?
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Completed training as a BTA, MTA, PTA, or CTA (biological, medical, pharmaceutical, or chemical technical assistant)
Completed training as a BTA, MTA, PTA, or CTA (biological, medical, pharmaceutical, or chemical technical assistant)
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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 - About the roleThe commercial project assistant role is a great opportunity to gain development within a dynamic and diverse team.
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 - About the roleThe commercial project assistant role is a great opportunity to gain development within a dynamic and diverse team.
NEU
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order to strengthen our development of a new, miniaturized infrared spectrometer, we are looking for you as an energetic Physical-Technical Assistant (PhyTA) who supports the R&D team with both hands in building up and running experiments, in maintaining instruments, in assembling high-tech components and by taking care that supplies do not run out.
order to strengthen our development of a new, miniaturized infrared spectrometer, we are looking for you as an energetic Physical-Technical Assistant (PhyTA) who supports the R&D team with both hands in building up and running experiments, in maintaining instruments, in assembling high-tech components and by taking care that supplies do not run out.
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Glosec * Siegen * Feste Anstellung * Vollzeit - Introduction - We are looking for a Machine & Plant Operator (m/f/d) to join our production, manufacturing and assembly team with immediate effect. * Independent operation and supply of fully automated assembly systems * Troubleshooting with root cause analysis * Measurement, assessment and documentation of processes and characteristics * System maintenance and servicing to the specified extent * Increasing system availability and output - Do you enjoy working on machines and are you interested in monitoring, controlling and operating them? * Completed vocational training * Experience in the operation and management of fully automated assembly systems * Willingness to work shifts in a three-shift system * Flexibility and commitment * Enjoyment of complex technical processes * Confident knowledge of German * Mobility is an advantage
Glosec * Siegen * Feste Anstellung * Vollzeit - Introduction - We are looking for a Machine & Plant Operator (m/f/d) to join our production, manufacturing and assembly team with immediate effect. * Independent operation and supply of fully automated assembly systems * Troubleshooting with root cause analysis * Measurement, assessment and documentation of processes and characteristics * System maintenance and servicing to the specified extent * Increasing system availability and output - Do you enjoy working on machines and are you interested in monitoring, controlling and operating them? * Completed vocational training * Experience in the operation and management of fully automated assembly systems * Willingness to work shifts in a three-shift system * Flexibility and commitment * Enjoyment of complex technical processes * Confident knowledge of German * Mobility is an advantage
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Schnelle Bewerbung
HEWI G. Winker GmbH & Co. KG * Spaichingen * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Area of responsibility * Operating and checking the tempering systems and hardness testers according to specifications * Maintenance and servicing of tempering systems 1 + 2 * General transport work (material supply, batch separation, production preparation) * Insertion of initial samples and production according to schedule * Carrying out tests during production - Professional requirements * Forklift licence * Professional experience in the field of heat treatment is an advantage * Good knowledge of scanner, PC - Knowledge and skills * Written and spoken German * Understanding of production processes * Ability to work in a team, flexibility - Your prospects with us * Attractive employer * Interesting, varied and challenging work * Secure and future-orientated workplace
HEWI G. Winker GmbH & Co. KG * Spaichingen * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Area of responsibility * Operating and checking the tempering systems and hardness testers according to specifications * Maintenance and servicing of tempering systems 1 + 2 * General transport work (material supply, batch separation, production preparation) * Insertion of initial samples and production according to schedule * Carrying out tests during production - Professional requirements * Forklift licence * Professional experience in the field of heat treatment is an advantage * Good knowledge of scanner, PC - Knowledge and skills * Written and spoken German * Understanding of production processes * Ability to work in a team, flexibility - Your prospects with us * Attractive employer * Interesting, varied and challenging work * Secure and future-orientated workplace
Schnelle Bewerbung
* HEWI G. Winker GmbH & Co. KG * Spaichingen * Feste Anstellung * Vollzeit Schnelle Bewerbung Area of responsibility * Management of the warehouse management system * Management of the driverless transport systems * Department-specific IT activities * Maintenance and servicing/repair of the system * Ensuring trouble-free operation of the system / AGV * Realisation of projects * Ensuring the tidiness and cleanliness of the entire system Professional requirements * Completed technical vocational training Knowledge and skills * Communication and team skills, flexibility * Confident handling of Microsoft Office package * Basic knowledge of ERP systems (Infor Xpert) would be desirable Your prospects with us * Attractive employer * Interesting, varied and challenging work * Secure and future-orientated workplace * Social benefits of a modern company
* HEWI G. Winker GmbH & Co. KG * Spaichingen * Feste Anstellung * Vollzeit Schnelle Bewerbung Area of responsibility * Management of the warehouse management system * Management of the driverless transport systems * Department-specific IT activities * Maintenance and servicing/repair of the system * Ensuring trouble-free operation of the system / AGV * Realisation of projects * Ensuring the tidiness and cleanliness of the entire system Professional requirements * Completed technical vocational training Knowledge and skills * Communication and team skills, flexibility * Confident handling of Microsoft Office package * Basic knowledge of ERP systems (Infor Xpert) would be desirable Your prospects with us * Attractive employer * Interesting, varied and challenging work * Secure and future-orientated workplace * Social benefits of a modern company
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Schnelle Bewerbung
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. * Proper handling, accountability and reconciliation of investigational products and clinical supplies. * Completed vocational training as a nurse ("Gesundheits- und Krankenpfleger/in" or "Pflegefachfrau/Pflegefachmann") or Medical Assistant ("MFA" = "Medizinische Fachangestellte"), or completed degree in a relevant field (e.g. health sciences, biology, pharmacy, public health)
The Milestone One Site Coordinator role supports a Clinical Study Site in clinical trial related activities according to ICH-GCP, protocol requirements within Study specific defined timelines and enrollment goals. We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery. * Proper handling, accountability and reconciliation of investigational products and clinical supplies. * Completed vocational training as a nurse ("Gesundheits- und Krankenpfleger/in" or "Pflegefachfrau/Pflegefachmann") or Medical Assistant ("MFA" = "Medizinische Fachangestellte"), or completed degree in a relevant field (e.g. health sciences, biology, pharmacy, public health)
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PTA (m/w/d) Voll- oder Teilzeit
PTA (m/w/d) Voll- oder Teilzeit
Pharmazeutix Apotheke in Ulzburg-Süd
Henstedt-Ulzburg
Teilweise Home-Office
Schnelle Bewerbung
Pharmazeutix Apotheke in Ulzburg-Süd * Henstedt-Ulzburg * Feste Anstellung * Homeoffice möglich, Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Description - We're working on behalf of a prestigious Chartered financial planning firm in Central London to find an experienced Paraplanner to join their growing team. Writing suitability reports across pensions, investments, and protection - Conducting research and cashflow modelling - Supporting with client strategies and technical analysis - Ensuring compliance and liaising with and clients - Diploma in Regulated Financial Planning (DipPFS or equivalent) 2+ years of experience as a Paraplanner within an IFA or wealth firm - Strong technical and report writing skills - Comfortable using platforms like Intelligent Office or FE Analytics - Paraplanner – Chartered Firm | London | Hybrid £45,000 – £55,000 + Bonus + Benefits - Permanent | Full-time |
Pharmazeutix Apotheke in Ulzburg-Süd * Henstedt-Ulzburg * Feste Anstellung * Homeoffice möglich, Teilzeit, Vollzeit - Sei einer der ersten Bewerber - Description - We're working on behalf of a prestigious Chartered financial planning firm in Central London to find an experienced Paraplanner to join their growing team. Writing suitability reports across pensions, investments, and protection - Conducting research and cashflow modelling - Supporting with client strategies and technical analysis - Ensuring compliance and liaising with and clients - Diploma in Regulated Financial Planning (DipPFS or equivalent) 2+ years of experience as a Paraplanner within an IFA or wealth firm - Strong technical and report writing skills - Comfortable using platforms like Intelligent Office or FE Analytics - Paraplanner – Chartered Firm | London | Hybrid £45,000 – £55,000 + Bonus + Benefits - Permanent | Full-time |
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Kymati GmbH * Grasbrunn * Feste Anstellung * Homeoffice möglich, Vollzeit - Join us at Kymati – Your career in the world of high-tech radar sensors in Munich! We are looking for talented people who want to shape the future with us and have fun doing it. Become part of our International Team and work on the development of high precision sensor solutions for industrial automation and aerospace solutions. Join us in shaping the next generation of industrial radar technology – with long-reaching vision: We are looking for a qualified and experienced engineer with expertise in high frequency radio signal generation. * Design, implement, and test waveforms for our radar applications on embedded hardware. * Perform signal processing from raw radar signals to classification and tracking. * Develop and provide radar solutions from scratch (concept in python) to embedded microcontrollers ...
Kymati GmbH * Grasbrunn * Feste Anstellung * Homeoffice möglich, Vollzeit - Join us at Kymati – Your career in the world of high-tech radar sensors in Munich! We are looking for talented people who want to shape the future with us and have fun doing it. Become part of our International Team and work on the development of high precision sensor solutions for industrial automation and aerospace solutions. Join us in shaping the next generation of industrial radar technology – with long-reaching vision: We are looking for a qualified and experienced engineer with expertise in high frequency radio signal generation. * Design, implement, and test waveforms for our radar applications on embedded hardware. * Perform signal processing from raw radar signals to classification and tracking. * Develop and provide radar solutions from scratch (concept in python) to embedded microcontrollers ...
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Schnelle Bewerbung
ST. ROBO GmbH * Berlin * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Tasks - At ST. ROBO, as a Technical Artist / Operator, you will play a critical role in the planning, setup, and operating of lighting and media systems for a variety of events and shows. You will work closely with our creative and technical teams to ensure seamless integration and flawless performance of our setups. Experience in touring and live entertainment productions is essential. * Operate and program lighting systems using Grand MA 2 & 3 consoles. * Manage and configure media servers using Disguise software. * Coordinate and execute lighting and media setups for touring and live entertainment productions. * Design and draft technical plans using Vectorworks. * Collaborate with to develop visual concepts and technical solutions. * Create and maintain diagrams and workflows using Lucid Chart.
ST. ROBO GmbH * Berlin * Feste Anstellung * Vollzeit - Schnelle Bewerbung - Tasks - At ST. ROBO, as a Technical Artist / Operator, you will play a critical role in the planning, setup, and operating of lighting and media systems for a variety of events and shows. You will work closely with our creative and technical teams to ensure seamless integration and flawless performance of our setups. Experience in touring and live entertainment productions is essential. * Operate and program lighting systems using Grand MA 2 & 3 consoles. * Manage and configure media servers using Disguise software. * Coordinate and execute lighting and media setups for touring and live entertainment productions. * Design and draft technical plans using Vectorworks. * Collaborate with to develop visual concepts and technical solutions. * Create and maintain diagrams and workflows using Lucid Chart.
Schnelle Bewerbung
Our Clinical Graduate Program is designed to help early-career professionals contribute to solutions that transform patient lives. As a part of the Field Clinical Specialist team, you'll play a crucial role in partnering with clinical professionals to deliver our patient-focused therapies including proctoring, training and education. The Clinical Graduate Program starts in October 2026, offering a structured 12-month fixed-term contract. * Intensive Educational Academy: Dive into a 12-month program that enhances your product knowledge, cardiovascular expertise, clinical understanding and fundamental commercial skills. * Hands-On Experience: Work alongside certified Field Clinical Specialists (FCS) to support case coverage, troubleshoot issues, program devices and follow up with patients on our cutting-edge product range.
Our Clinical Graduate Program is designed to help early-career professionals contribute to solutions that transform patient lives. As a part of the Field Clinical Specialist team, you'll play a crucial role in partnering with clinical professionals to deliver our patient-focused therapies including proctoring, training and education. The Clinical Graduate Program starts in October 2026, offering a structured 12-month fixed-term contract. * Intensive Educational Academy: Dive into a 12-month program that enhances your product knowledge, cardiovascular expertise, clinical understanding and fundamental commercial skills. * Hands-On Experience: Work alongside certified Field Clinical Specialists (FCS) to support case coverage, troubleshoot issues, program devices and follow up with patients on our cutting-edge product range.
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Senior Clinical Trial Project Manager MD (m/f/d) 80–100%
Senior Clinical Trial Project Manager MD (m/f/d) 80–100%
regenold GmbH
bundesweit, Home-Office
Teilweise Home-Office
Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications * 6+ years of hands-on experience in managing clinical trials with solid experience in clinical investigations - In this client-facing consulting role, as part of the you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors. * Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field * Managing clinical investigations end to end, from study planning to close-out * Proven track record in such as (Senior) Clinical Project Manager / Lead, ideally across different settings (Pharma, CRO) * Profound knowledge of GCP and the clinical regulatory environment
Preparing and submitting Clinical Trial Applications and managing requests and deficiency communications * 6+ years of hands-on experience in managing clinical trials with solid experience in clinical investigations - In this client-facing consulting role, as part of the you will take full responsibility for the setup and operational management of clinical investigations on behalf of our clients in the medical device and IVD sectors. * Taking responsibility for the setup and operational delivery of clinical investigations for regenold clients in the medical device and IVD field * Managing clinical investigations end to end, from study planning to close-out * Proven track record in such as (Senior) Clinical Project Manager / Lead, ideally across different settings (Pharma, CRO) * Profound knowledge of GCP and the clinical regulatory environment
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Field Clinical Specialist TMTT – Baden‑Württemberg
Field Clinical Specialist TMTT – Baden‑Württemberg
Edwards Lifesciences GmbH
Baden-Württemberg
Teilweise Home-Office
Schnelle Bewerbung
• Provide feedback to improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP - Develops clinical education materials in connection with clinical investigations. Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clinical investigation. • Perform routine reviews on clinical support activities, changes in the market and assigned accounts, as well as, competitive activity with cross-functional teams (e.g., sales) Bachelor's Degree in in related field Training experience in clinical / technical environment Required - Other: 3 year experience of previous related medical device and/or clinical experience Required
• Provide feedback to improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP - Develops clinical education materials in connection with clinical investigations. Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clinical investigation. • Perform routine reviews on clinical support activities, changes in the market and assigned accounts, as well as, competitive activity with cross-functional teams (e.g., sales) Bachelor's Degree in in related field Training experience in clinical / technical environment Required - Other: 3 year experience of previous related medical device and/or clinical experience Required
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As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. The Application Specialist Clinical Microbiology North Germany (d/f/m) for Beckman Coulter Diagnostics is responsible for ensuring successful implementation and utilization of our microbiology diagnostics instruments and solutions. * Serve as a subject matter expert in clinical microbiology, demonstrating a deep understanding of laboratory procedures, protocols, and best practices.
As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence. The Application Specialist Clinical Microbiology North Germany (d/f/m) for Beckman Coulter Diagnostics is responsible for ensuring successful implementation and utilization of our microbiology diagnostics instruments and solutions. * Serve as a subject matter expert in clinical microbiology, demonstrating a deep understanding of laboratory procedures, protocols, and best practices.
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Clinical Research - Head of Gastroenterology II (m/f/d)
Clinical Research - Head of Gastroenterology II (m/f/d)
Dr. Falk Pharma GmbH
Freiburg im Breisgau
Teilweise Home-Office
Schnelle Bewerbung
Serves as group lead (GL) for the company-sponsored clinical trials and development programs in the therapeutic area of functional gastrointestinal and gastrointestinal motility disorders. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials within this therapeutic area. * Review and approval of critical development documents (e.g., Clinical Trial Protocol, master ICF, Statistical Analysis Plan, Clinical Trial Protocol) * Significant experience with clinical evaluation projects including the development of Clinical Trial Protocols, case report forms, Informed Consent Forms and Investigator Brochures. * Solid knowledge of regulatory requirements for conducting clinical trials * Several years of management experience - GL collaborates with Clinical Research teams from other therapeutic areas and serves as a key liaison ...
Serves as group lead (GL) for the company-sponsored clinical trials and development programs in the therapeutic area of functional gastrointestinal and gastrointestinal motility disorders. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials within this therapeutic area. * Review and approval of critical development documents (e.g., Clinical Trial Protocol, master ICF, Statistical Analysis Plan, Clinical Trial Protocol) * Significant experience with clinical evaluation projects including the development of Clinical Trial Protocols, case report forms, Informed Consent Forms and Investigator Brochures. * Solid knowledge of regulatory requirements for conducting clinical trials * Several years of management experience - GL collaborates with Clinical Research teams from other therapeutic areas and serves as a key liaison ...
Field Clinical Specialist TMTT, Bonn/Siegen
Field Clinical Specialist TMTT, Bonn/Siegen
Edwards Lifesciences GmbH
Bonn, Siegen
Teilweise Home-Office
Schnelle Bewerbung
Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. Your insight and dedication will help deepen and broaden clinical knowledge of our company's innovative technologies, while creating connections between and teams across our businesses to ensure patients receive the highest quality of care. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. * Regularly reviews clinical support activities and changes in the market & assigned accounts * Bachelor's Degree in related field (Biomedical Engineering or Nursing) and training experience in clinical / technical environment is required. * Clinical experience is beneficial
Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP. Your insight and dedication will help deepen and broaden clinical knowledge of our company's innovative technologies, while creating connections between and teams across our businesses to ensure patients receive the highest quality of care. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. * Regularly reviews clinical support activities and changes in the market & assigned accounts * Bachelor's Degree in related field (Biomedical Engineering or Nursing) and training experience in clinical / technical environment is required. * Clinical experience is beneficial
Field Clinical Specialist - Imaging
Field Clinical Specialist - Imaging
Edwards Lifesciences GmbH
Nordrhein-Westfalen, Rheinland-Pfalz
Teilweise Home-Office
Schnelle Bewerbung
Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. The Field Clinical Specialist - Imaging is responsible for educating physicians on EVOQUE technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals / in assigned territories / regions. * Analyze, summarize, and present clinical baseline, procedural, and follow-up imaging (e.g., CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations * Provide on-site cardiac imaging support and guidance during clinical procedures to ensure optimal imaging during the implantation of transcatheter devices (if certified). * Bachelor's Degree in in technical field (e.g., clinical physiology, ...
Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. The Field Clinical Specialist - Imaging is responsible for educating physicians on EVOQUE technologies, device handling, implantation and troubleshooting techniques and case support by assigned hospitals / in assigned territories / regions. * Analyze, summarize, and present clinical baseline, procedural, and follow-up imaging (e.g., CT, echo, MRI, angiography) to provide inputs that support new product and procedure development and to support event investigations * Provide on-site cardiac imaging support and guidance during clinical procedures to ensure optimal imaging during the implantation of transcatheter devices (if certified). * Bachelor's Degree in in technical field (e.g., clinical physiology, ...
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Representation of clinical practice within product development projects * Support of clinical validation and testing activities * Structured collection and provision of clinical feedback on existing products * Building and maintaining a professional clinical network in emergency and respiratory care * Close collaboration with Product Management, Research & Development, and an international Clinical Application Specialist network * Completed clinical training as a paramedic (preferred), ideally complemented by qualification as a critical care nurse or a comparable advanced certification
Representation of clinical practice within product development projects * Support of clinical validation and testing activities * Structured collection and provision of clinical feedback on existing products * Building and maintaining a professional clinical network in emergency and respiratory care * Close collaboration with Product Management, Research & Development, and an international Clinical Application Specialist network * Completed clinical training as a paramedic (preferred), ideally complemented by qualification as a critical care nurse or a comparable advanced certification
Field Clinical Specialist Münster - Hannover
Field Clinical Specialist Münster - Hannover
Edwards Lifesciences GmbH
Bielefeld, Münster, Hannover
Teilweise Home-Office
Schnelle Bewerbung
Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP - Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Field Clinical Specialists will provide guidance on the use of the device, thereby enabling physicians and staff to reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. * Working independently in the areas of valve crimping, case management, pre-case planning, ...
Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP - Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. Field Clinical Specialists will provide guidance on the use of the device, thereby enabling physicians and staff to reach expert proficiency and deliver positive patient outcomes. This role will collaborate with multiple departments including Sales, Clinical Affairs, Marketing, Quality, Regulatory, and Education. After extensive training, a Field Clinical Specialist will travel frequently within an assigned territory, clinically training customers on the THV technology. * Working independently in the areas of valve crimping, case management, pre-case planning, ...
Clinical Project Manager Early Clinical Research - Pharmacology (m/f/d)
Clinical Project Manager Early Clinical Research - Pharmacology (m/f/d)
Dr. Falk Pharma GmbH
Freiburg
Teilweise Home-Office
Schnelle Bewerbung
Strategic planning, execution, and oversight of international Phase I clinical trials in accordance with GCP/ICH-GCP guidelines, regulatory requirements (EMA/FDA), and internal SOPs * Solid knowledge of regulatory requirements for conducting clinical trials * Excellent knowledge of MS Office applications * Analysis and interpretation of study results as well as review and assessment of clinical study reports * Supporting the clinical research department with questions related to clinical pharmacology * Supporting the preparation of regulatory submissions and handling regulatory inquiries on clinical pharmacology topics * Several years of professional experience in the pharmaceutical industry in clinical development and clinical study project management, ideally in Phase I * Experience in clinical pharmacology (pharmacokinetics, pharmacodynamics)
Strategic planning, execution, and oversight of international Phase I clinical trials in accordance with GCP/ICH-GCP guidelines, regulatory requirements (EMA/FDA), and internal SOPs * Solid knowledge of regulatory requirements for conducting clinical trials * Excellent knowledge of MS Office applications * Analysis and interpretation of study results as well as review and assessment of clinical study reports * Supporting the clinical research department with questions related to clinical pharmacology * Supporting the preparation of regulatory submissions and handling regulatory inquiries on clinical pharmacology topics * Several years of professional experience in the pharmaceutical industry in clinical development and clinical study project management, ideally in Phase I * Experience in clinical pharmacology (pharmacokinetics, pharmacodynamics)
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Schnelle Bewerbung
To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out * Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders * Contribute to continuous process improvement initiatives, including SOP development and implementation of best practices in clinical operations * 7–10+ years of experience in clinical research, including clinical project management
To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Lead the end-to-end management of clinical studies for Class III medical devices, from feasibility assessment through study close-out * Develop, maintain, and track clinical project plans, timelines, budgets, and risk management strategies * Ensure all clinical studies are conducted in compliance with GCP (ISO 14155), EU MDR, and applicable local regulatory requirements * Coordinate and collaborate with cross-functional teams, including Data Management, Clinical Research Associates (CRAs), and other relevant internal stakeholders * Contribute to continuous process improvement initiatives, including SOP development and implementation of best practices in clinical operations * 7–10+ years of experience in clinical research, including clinical project management
Schnelle Bewerbung
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. * Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents * Provides medical risk assessment for activities related to clinical trials and development programs * Performs oversight for clinical trial medical monitoring activities outsourced to CROs * Point of contact for sites and clinical trial teams with medical questions
Serves as medical lead (ML) for the company-sponsored clinical trials and development programs. Responsible for guiding the clinical development strategy and ensuring the scientific integrity of clinical trials. ML manages all medical aspects of clinical trials and contributes to the development of trial documents. * Provides medical input to Clinical Trial Protocol, Investigator's Brochure, Informed Consent Form, Independent Data Monitoring Committee Charter, Statistical Analysis Plan, Medical Monitoring Plan, Clinical Trial Report, Clinical Trial Overview Statements and other clinical trial documents * Provides medical risk assessment for activities related to clinical trials and development programs * Performs oversight for clinical trial medical monitoring activities outsourced to CROs * Point of contact for sites and clinical trial teams with medical questions
Beliebte Jobs
Standorte
- Berlin
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