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27 Treffer für Clinical Expert Jobs in Planegg im Umkreis von 30 km
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Schnelle Bewerbung
We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. 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 ...
We are seeking a senior Clinical Pharmacology expert who can combine deep pharmaceutical industry experience with a strong understanding of regulatory authority expectations. HMNC Brain Health (HMNC) is a clinical-stage neuroscience company pioneering new therapies for mental health disorders. 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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Schnelle Bewerbung
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research - 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 SAS programming * Expert knowledge and understanding of CDISC ADaM standard * Expert knowledge and understanding of adaptive designs * Expert knowledge and understanding of sample size calculation * Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH) * Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, ...
Expert knowledge and understanding of the statistical principles, concepts, methods, and standards used in clinical research - 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 SAS programming * Expert knowledge and understanding of CDISC ADaM standard * Expert knowledge and understanding of adaptive designs * Expert knowledge and understanding of sample size calculation * Expert knowledge and understanding of relevant regulations and guidelines (e.g. FDA, EMA, ICH) * Ability to apply advanced statistical techniques in support of clinical research studies and to analyze, interpret, ...
Noch nichts dabei? Es gibt 25 weitere Jobs, die zu deiner Suche passen könnten
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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
Optionally providing support during audits of clinical processes of as a clinial expert (remote or on-site) * 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 * 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.
Optionally providing support during audits of clinical processes of as a clinial expert (remote or on-site) * 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 * 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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Director (gn) Portfolio Management, Market Analysis & Strategic Projects
Director (gn) Portfolio Management, Market Analysis & Strategic Projects
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.
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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 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. * 10+ years of experience in clinical safety and pharmacovigilance, including senior medical safety role - You have solid knowledge of global clinical safety and pharmacovigilance ...
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. * 10+ years of experience in clinical safety and pharmacovigilance, including senior medical safety role - You have solid knowledge of global clinical safety and pharmacovigilance ...
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In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. 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.
In a spacious modern setting full of opportunities for further development, ZEISS employees work in a place where expert knowledge and team spirit reign supreme. 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.
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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
Mitarbeit in kundenspezifischen Arbeitsgruppen und anderen internen Projekten als Subject Matter Expert
Mitarbeit in kundenspezifischen Arbeitsgruppen und anderen internen Projekten als Subject Matter Expert
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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
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. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS).
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. * Collaborates with development and maintenance of Clinical Trial Management System (CTMS).
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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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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
The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion's product/s across the product/s life cycle. He/she is a peer scientific expert who communicates accurate and applicable science to (KOLs) within a geographic area. He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. Develop and continuously maintain the highest scientific and medical expertise in the field of adult and pediatric bone, liver and metabolic diseases, and adjacent specialties (e.g., endocrinology, osteology, rheumatology, orthopedics, radiology, laboratory medicine, pediatric gastroenterology) especially in areas which affect Alexion (Hypophosphatasia, Lysosomal acid lipase deficiency) and be acknowledged internally and externally as an expert in these areas.
The Medical Science Liaison (MSL) is a field-based scientific expert that strategically supports the medical and scientific objectives of Alexion's product/s across the product/s life cycle. He/she is a peer scientific expert who communicates accurate and applicable science to (KOLs) within a geographic area. He/she combines strong business acumen and clinical expertise and serves as a peer-to-peer liaison internally and externally. Develop and continuously maintain the highest scientific and medical expertise in the field of adult and pediatric bone, liver and metabolic diseases, and adjacent specialties (e.g., endocrinology, osteology, rheumatology, orthopedics, radiology, laboratory medicine, pediatric gastroenterology) especially in areas which affect Alexion (Hypophosphatasia, Lysosomal acid lipase deficiency) and be acknowledged internally and externally as an expert in these areas.
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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. * Provide expert advice to corporate functions on drug safety requirements and best practices.
Partner across Patient Safety to drive compliance for post-marketing and clinical trial safety activities and uphold company policies and standards. * Provide expert advice to corporate functions on drug safety requirements and best practices.
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Associate Director Regulatory Affairs – Clinical Lead*
Associate Director Regulatory Affairs – Clinical Lead*
Immatics Biotechnologies GmbH
Tübingen, München, Home-Office
Teilweise Home-Office
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications. * Demonstrated experience leading EU regulatory strategy for clinical-stage programs.
We are currently seeking an Associate Director Regulatory Affairs – Clinical Lead* to strengthen our EU Regulatory team. You will independently lead EU regulatory activities for assigned clinical programs and act as a of regulatory strategy and execution. * Drive initial clinical trial application and its lifecycle management, including major Substantial Modifications, with a proactive and risk-based mindset. This includes preparation, review and maintaining documentation of clinical trial applications. * Demonstrated experience leading EU regulatory strategy for clinical-stage programs.
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Gesundheits- und Krankenpfleger in der Gesundheitsberatung (m/w/d)
Gesundheits- und Krankenpfleger in der Gesundheitsberatung (m/w/d)
SHL Telemedizin GmbH
München
Teilweise Home-Office
Du bist sicher im Umgang mit digitalen Tools (MS Office, idealerweise Clinical Portals) und besitzt eine hohe Technikaffinität
Du bist sicher im Umgang mit digitalen Tools (MS Office, idealerweise Clinical Portals) und besitzt eine hohe Technikaffinität
In Computational Pathology and Biomarkers, we deliver AI-driven solutions for patient selection, biomarker development, and clinical decisions on a scale. Do you thrive at the intersection of AI innovation and clinical translation? In this role, you will collaborate with multidisciplinary teams to data-driven approaches that generate impactful insights and improve clinical outcomes. Working at the intersection of data, AI innovation, and tumor biology, you will collaborate in cross-functional teams to develop and implement computational pathology solutions from early discovery through clinical validation, generating high-quality translational insights that support critical decisions and advance precision medicine. * Apply deep understanding of cancer biology to interpret clinical samples, support rational drug combinations, and identify mechanisms of resistance.
In Computational Pathology and Biomarkers, we deliver AI-driven solutions for patient selection, biomarker development, and clinical decisions on a scale. Do you thrive at the intersection of AI innovation and clinical translation? In this role, you will collaborate with multidisciplinary teams to data-driven approaches that generate impactful insights and improve clinical outcomes. Working at the intersection of data, AI innovation, and tumor biology, you will collaborate in cross-functional teams to develop and implement computational pathology solutions from early discovery through clinical validation, generating high-quality translational insights that support critical decisions and advance precision medicine. * Apply deep understanding of cancer biology to interpret clinical samples, support rational drug combinations, and identify mechanisms of resistance.
Director (gn) Business Development - Licensing & Alliance Management
Director (gn) Business Development - Licensing & Alliance Management
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.
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Senior Scientist (m/f/d), Computational Pathology Biomarker Lead (BioPharmaceuticals)
Senior Scientist (m/f/d), Computational Pathology Biomarker Lead (BioPharmaceuticals)
AstraZeneca
München
Within Computational Pathology and Biomarkers, we develop AI-powered solutions to advance patient selection, biomarker development, and clinical decision-making at scale. Do you thrive at the intersection of AI, biology, and clinical translation? In this role, you will collaborate with cross-functional teams to generate data-driven insights that inform clinical decisions across therapeutic areas such as cardiovascular, renal, metabolic, and respiratory diseases. Work at the interface of biology, data science, and AI to generate actionable insights throughout drug development - from target validation to clinical implementation. * Design and apply computational pathology and AI approaches across diverse tissue types, disease areas, and clinical endpoints * Support analytical and clinical validation to enable biomarker implementation in clinical studies
Within Computational Pathology and Biomarkers, we develop AI-powered solutions to advance patient selection, biomarker development, and clinical decision-making at scale. Do you thrive at the intersection of AI, biology, and clinical translation? In this role, you will collaborate with cross-functional teams to generate data-driven insights that inform clinical decisions across therapeutic areas such as cardiovascular, renal, metabolic, and respiratory diseases. Work at the interface of biology, data science, and AI to generate actionable insights throughout drug development - from target validation to clinical implementation. * Design and apply computational pathology and AI approaches across diverse tissue types, disease areas, and clinical endpoints * Support analytical and clinical validation to enable biomarker implementation in clinical studies
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Vertriebsleiter (m/w/d) Medizintechnik DACH
Vertriebsleiter (m/w/d) Medizintechnik DACH
ACANDIS GmbH
Stuttgart, München, Frankfurt am Main, Nürnberg, Pforzheim
Schnelle Bewerbung
Enge Zusammenarbeit mit Marketing, Produktmanagement und Clinical Support
Enge Zusammenarbeit mit Marketing, Produktmanagement und Clinical Support
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.
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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
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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
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
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.
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).
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.
Beliebte Jobs
- Arzt
- Pharmareferent Ausbildung
- Physiotherapeut Ausbildung
- Industriekaufmann Ausbildung
- Logopädie Ausbildung
- Kommunikation
- Pflegehelfer Ausbildung
- Finanzen
- Tierarzt Ausbildung
- Arzt Ausbildung
- Rettungssanitäter Ausbildung
- Kfz Mechaniker Ausbildung
- Heilpraktiker Ausbildung
- MFA Ausbildung
- English Speaking
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