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                          16 resultaten voor Clinical monitor in Olen binnen een straal van 30 km

                          Senior Clinical Research Associate (Site Manager)

                          Johnson & Johnson
                          2340 Beerse, Belgium
                          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
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                          We hebben je zoekopdracht uitgebreid met 15 gelijkaardige vacatures.

                          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.
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                          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
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                          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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                          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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                          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
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                          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.
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                          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.
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                          We hebben je zoekopdracht uitgebreid met 9 vacatures buiten de geselecteerde regio

                          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.
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                          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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                          As a Development Analyst, you will provide scientific expertise to contribute to manage physico-chemical method development activities for Biologicals Products from early clinical phases to commercial.
                          As a Development Analyst, you will provide scientific expertise to contribute to manage physico-chemical method development activities for Biologicals Products from early clinical phases to commercial.
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                          Wat is het gemiddelde salaris voor Clinical monitor in Olen?

                          Gemiddeld salaris per jaar
                          42.200 €

                          Het salaris gemiddelde voor een Clinical monitor in Olen is 42.200 €. De salarissen van Clinical monitor in Olen variëren van 35.200 € tot 51.200 €.