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11
19 resultaten voor Clinical monitor in Oevel binnen een straal van 30 km
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
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Johnson & Johnson is currently seeking two Senior Clinical Research Associates (Site Manager) to join our Global Clinical Operations team. One Senior Clinical Research Associates (Site Manager) will be located in Breda, Netherlands and the second one in Beerse, Belgium. You will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. You will collaborate with the Local (LTM), Clinical Trial Assistant (CTA), and Clinical Trial Manager (CTM) to ensure overall site management while performing trial-related activities for assigned protocols. A minimum of 3 years of clinical trial monitoring
Johnson & Johnson is currently seeking two Senior Clinical Research Associates (Site Manager) to join our Global Clinical Operations team. One Senior Clinical Research Associates (Site Manager) will be located in Breda, Netherlands and the second one in Beerse, Belgium. You will be assigned to trial sites to ensure compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), as well as applicable regulations and guidelines. You will collaborate with the Local (LTM), Clinical Trial Assistant (CTA), and Clinical Trial Manager (CTM) to ensure overall site management while performing trial-related activities for assigned protocols. A minimum of 3 years of clinical trial monitoring
We hebben je zoekopdracht uitgebreid met 17 gelijkaardige vacatures.
As a Site Technology Specialist, you will work with clinical sites and provide technical support and expertise related to technology (Kidney imaging, cell therapy, radiology and renal ultrasounds) * Provide clinical sites with technical support and expertise related to technology (Nuclear medicine, kidney imaging, interventional radiology) * Assist and advises the site monitor in the area of study technologies
As a Site Technology Specialist, you will work with clinical sites and provide technical support and expertise related to technology (Kidney imaging, cell therapy, radiology and renal ultrasounds) * Provide clinical sites with technical support and expertise related to technology (Nuclear medicine, kidney imaging, interventional radiology) * Assist and advises the site monitor in the area of study technologies
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Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
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Vacature Clinical trial assistant neuromusculaire aandoeningen UZ LEUVEN in Leuven
Vacature Clinical trial assistant neuromusculaire aandoeningen UZ LEUVEN in Leuven
UZ Leuven
Leuven, België
Wij zijn op zoek naar een enthousiaste en gedreven clinical trial assistant om ons team te versterken.
Wij zijn op zoek naar een enthousiaste en gedreven clinical trial assistant om ons team te versterken.
NIEUW
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Dobit * 2250 Olen, België - Solliciteer als één van de eersten - Jobomschrijving * Na een interne productspecifieke opleiding, word je het aanspreekpunt voor de begeleiding en ondersteuning van gebruikers doorheen de verschillende gerealiseerde projecten. * Als IT Support Engineer heb je een zeer gevarieerde job, je behandelt inkomende supporttickets en analyseert uiteenlopende hardware, software- en systeemvraagstukken. * Op een betrokken wijze garandeer je een oplossing, verkregen door relevante en accurate vragen of het toewijzen van interne specialisten. * Je plant indien nodig interventies in en ondersteunt de in hun interventies. De coördinatie, communicatie en administratieve opvolging blijft bij jou! Jouw profiel * Je beschikt over een goede algemene IT-kennis: Windows, hardware, basis netwerkbegrip; een diploma in de informatica/ICT is een plus.
Dobit * 2250 Olen, België - Solliciteer als één van de eersten - Jobomschrijving * Na een interne productspecifieke opleiding, word je het aanspreekpunt voor de begeleiding en ondersteuning van gebruikers doorheen de verschillende gerealiseerde projecten. * Als IT Support Engineer heb je een zeer gevarieerde job, je behandelt inkomende supporttickets en analyseert uiteenlopende hardware, software- en systeemvraagstukken. * Op een betrokken wijze garandeer je een oplossing, verkregen door relevante en accurate vragen of het toewijzen van interne specialisten. * Je plant indien nodig interventies in en ondersteunt de in hun interventies. De coördinatie, communicatie en administratieve opvolging blijft bij jou! Jouw profiel * Je beschikt over een goede algemene IT-kennis: Windows, hardware, basis netwerkbegrip; een diploma in de informatica/ICT is een plus.
Are you interested in becoming part of a dynamic team that drives clinical trial activities in Belgium and The Netherlands and operates in an international environment? We are looking for a driven Director Clinical Operations to lead our growing oncology team in Global Clinical Operations in Belgium and The Netherlands . In this vital role, you will be accountable for delivery of the oncology portfolio while leading a team of Clinical Operations, while focusing on enhancing staff performance, professional development, training, onboarding, and resource management to ensure the seamless execution of clinical trials from feasibility through study close-out (2nd line leader). Help shape the clinical trial environment by partnering with health authorities, ethics committe
Are you interested in becoming part of a dynamic team that drives clinical trial activities in Belgium and The Netherlands and operates in an international environment? We are looking for a driven Director Clinical Operations to lead our growing oncology team in Global Clinical Operations in Belgium and The Netherlands . In this vital role, you will be accountable for delivery of the oncology portfolio while leading a team of Clinical Operations, while focusing on enhancing staff performance, professional development, training, onboarding, and resource management to ensure the seamless execution of clinical trials from feasibility through study close-out (2nd line leader). Help shape the clinical trial environment by partnering with health authorities, ethics committe
We are searching for the best talent for aSenior Manager, Clinical Trial Learning & Training (CTL&T) to be in Beerse, Belgium; Madrid, Spain; or Warsaw, Poland. The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. * Serves as a key contact for the GCO Organization for training and learning for functional training and for Global Development specific to clinical trial training. * Well-developed skills and knowledge of core business processes and practices (i.e., SOPs and Systems governing clinical research activities)
We are searching for the best talent for aSenior Manager, Clinical Trial Learning & Training (CTL&T) to be in Beerse, Belgium; Madrid, Spain; or Warsaw, Poland. The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. * Serves as a key contact for the GCO Organization for training and learning for functional training and for Global Development specific to clinical trial training. * Well-developed skills and knowledge of core business processes and practices (i.e., SOPs and Systems governing clinical research activities)
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Monitor operational KPIs and initiate corrective actions when needed.
Monitor operational KPIs and initiate corrective actions when needed.
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Working closely with the , you will guide key quality activities, monitor performance indicators, and act on critical product decisions to ensure the site's overall reliability and consistency.
Working closely with the , you will guide key quality activities, monitor performance indicators, and act on critical product decisions to ensure the site's overall reliability and consistency.
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● Cascades and monitors KPIs to deliver expected performance benefits.
● Cascades and monitors KPIs to deliver expected performance benefits.
The PLD team is at the forefront of innovation, developing Parenteral and Liquid drug product formulations and processes across our R&D Synthetics portfolio (small molecules, peptides, oligonucleotides, drug conjugates), from late discovery through preclinical and clinical development, and into commercialization. You will be involved in experimental design, formulation engineering, process optimization, scale-up, and technology transfer for clinical trial manufacturing. Provide input for master batch records for clinical batches; perform criticality analysis and define control strategies.
The PLD team is at the forefront of innovation, developing Parenteral and Liquid drug product formulations and processes across our R&D Synthetics portfolio (small molecules, peptides, oligonucleotides, drug conjugates), from late discovery through preclinical and clinical development, and into commercialization. You will be involved in experimental design, formulation engineering, process optimization, scale-up, and technology transfer for clinical trial manufacturing. Provide input for master batch records for clinical batches; perform criticality analysis and define control strategies.
A blend of creativity and analytical skills: you're able to both create compelling marketing content and to monitor and optimize it, figuring out what works and why.
A blend of creativity and analytical skills: you're able to both create compelling marketing content and to monitor and optimize it, figuring out what works and why.
Je werkt graag samen in een multidisciplinair team waar ook artsen, clinical support managers, business managers deel van uitmaken en kan technische concepten op een heldere manier uitleggen aan deze stakeholders.
Je werkt graag samen in een multidisciplinair team waar ook artsen, clinical support managers, business managers deel van uitmaken en kan technische concepten op een heldere manier uitleggen aan deze stakeholders.
Monitor results to refine budget allocation and campaign strategy
Monitor results to refine budget allocation and campaign strategy
Launch and monitor the implementation of awarded contracts in collaboration with the legal department.
Launch and monitor the implementation of awarded contracts in collaboration with the legal department.
Monitor sales performance against budget and forecasts, delivering actionable insights by region and product line.
Monitor sales performance against budget and forecasts, delivering actionable insights by region and product line.
NIEUW
Together with the system engineers, you define the mechanical requirements, monitor progress and quality criteria, and jointly evaluate the final product during acceptance
Together with the system engineers, you define the mechanical requirements, monitor progress and quality criteria, and jointly evaluate the final product during acceptance
We hebben je zoekopdracht uitgebreid met 9 vacatures buiten de geselecteerde regio
Clinical Applications - Solution Area Specialist - Dutch Speaking
Clinical Applications - Solution Area Specialist - Dutch Speaking
Microsoft
Multiple Locations, Belgium
You will showcase the value proposition of Dragon Copilot in improving clinical documentation, provider efficiency, and patient outcomes. * You will serve as a knowledge leader in the role of AI-powered clinical documentation across diverse healthcare organizations, including hospitals, academic institutions, and large healthcare systems. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as Chief Medical Information Officers (CMIO), Chief Information Officers (CIO), Chief Nursing Officers (CNO), and departmental directors involved in clinical documentation and workflow optimization.
You will showcase the value proposition of Dragon Copilot in improving clinical documentation, provider efficiency, and patient outcomes. * You will serve as a knowledge leader in the role of AI-powered clinical documentation across diverse healthcare organizations, including hospitals, academic institutions, and large healthcare systems. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as Chief Medical Information Officers (CMIO), Chief Information Officers (CIO), Chief Nursing Officers (CNO), and departmental directors involved in clinical documentation and workflow optimization.
Monitor HR Consulting
Monitor HR Consulting
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Building a qualified pipeline across Europe (Pharma, Biotech, Clinical Trials, Diagnostics, 3PLs, High-Value Food)
Building a qualified pipeline across Europe (Pharma, Biotech, Clinical Trials, Diagnostics, 3PLs, High-Value Food)
You will have the opportunity to travel to monitor the progress of your projects and create new business opportunities (approximately 25% of the time, with an average 1-week field mission).
You will have the opportunity to travel to monitor the progress of your projects and create new business opportunities (approximately 25% of the time, with an average 1-week field mission).
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You will monitor relevant legislation proactively, inform management and make proposals for implementation
You will monitor relevant legislation proactively, inform management and make proposals for implementation
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Als entrepreneur zie je continu nieuwe kansen maar monitor je ook voldoende de risico's van ons klantenbestand.
Als entrepreneur zie je continu nieuwe kansen maar monitor je ook voldoende de risico's van ons klantenbestand.