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9 results for Senior Clinical Research Manager jobs in Turnhout within a 30 km radius
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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 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 experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager 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.
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 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 experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager 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.
No match yet? There are 8 more jobs that could match your search
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FUNCTIE Als Research Engineer Human AI promoot je deze innovatieve technologieën en breng je de grenzen van bestaande marktoplossingen in kaart.
FUNCTIE Als Research Engineer Human AI promoot je deze innovatieve technologieën en breng je de grenzen van bestaande marktoplossingen in kaart.
Minimum of 12 years of clinical research experience acquired in pharmaceutical industry, CRO or investigational site. Excellent knowledge of drug development, clinical research operations and regulatory requirements including ICH-GCP, HCC and applicable regulations. Influential in improving the clinical research environment at a country level. 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? Would you like to embrace your skills as a people manager in an innovative healthcare company, while driving strategy and portfolio delivery? We are looking for a driven Director Clinical Operations to lead our g
Minimum of 12 years of clinical research experience acquired in pharmaceutical industry, CRO or investigational site. Excellent knowledge of drug development, clinical research operations and regulatory requirements including ICH-GCP, HCC and applicable regulations. Influential in improving the clinical research environment at a country level. 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? Would you like to embrace your skills as a people manager in an innovative healthcare company, while driving strategy and portfolio delivery? We are looking for a driven Director Clinical Operations to lead our g
The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. 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 will engage with key , vendors, and teams/peers responsible for training creation, facilitation, and delivery. * Well-developed skills and knowledge of core business processes and practices (i.e., SOPs and Systems governing clinical research activities) * Keeps abreast of training and development research within/out of industry, new materials, methodologies. * Serves as a key c
The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. 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 will engage with key , vendors, and teams/peers responsible for training creation, facilitation, and delivery. * Well-developed skills and knowledge of core business processes and practices (i.e., SOPs and Systems governing clinical research activities) * Keeps abreast of training and development research within/out of industry, new materials, methodologies. * Serves as a key c
J&J Innovative Medicine Research & Development develops treatments that improve the health and lifestyles of people worldwide. 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. The role includes hands-on lab-based research activities, while offering leadership and growth opportunities. Provide input for master batch records for clinical batches; perform criticality an
J&J Innovative Medicine Research & Development develops treatments that improve the health and lifestyles of people worldwide. 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. The role includes hands-on lab-based research activities, while offering leadership and growth opportunities. Provide input for master batch records for clinical batches; perform criticality an
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EYETEC is een Europese referentiespeler in het leveren van diensten en machines in de farmaceutische sector (productie, research en ziekenhuizen).
EYETEC is een Europese referentiespeler in het leveren van diensten en machines in de farmaceutische sector (productie, research en ziekenhuizen).
The Category Manager is responsible for Category Management, Strategic sourcing and negotiation, Contract Management and Risk Management of all TKI assigned commodities. * Conduct research on supplier market dynamics, cost drivers, supplier business models, total cost of ownership models and historical spend to enhance future negotiations.
The Category Manager is responsible for Category Management, Strategic sourcing and negotiation, Contract Management and Risk Management of all TKI assigned commodities. * Conduct research on supplier market dynamics, cost drivers, supplier business models, total cost of ownership models and historical spend to enhance future negotiations.
We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.
We embrace research and science -- bringing innovative ideas, products and services to advance the health and well-being of people.
At Intersoft Electronics, we are looking for a Technical Writer to join our team and help communicate our cutting-edge research and radar technology solutions. You will play a key role in writing grant proposals, documenting research output, and creating system-level documentation for our customers. * Document research results and scientific publications.
At Intersoft Electronics, we are looking for a Technical Writer to join our team and help communicate our cutting-edge research and radar technology solutions. You will play a key role in writing grant proposals, documenting research output, and creating system-level documentation for our customers. * Document research results and scientific publications.
6 exact matches jobs are outside your preferred location
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. * Collaborate proactively and strategically with the core account team—including Account Executives, Customer Success Managers, and Technical Specialists—to align on account plans, drive joint sales motions, and ensure seamless execution of solution strategies for healthcare clients in Strategic, Major & Education markets. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as
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. * Collaborate proactively and strategically with the core account team—including Account Executives, Customer Success Managers, and Technical Specialists—to align on account plans, drive joint sales motions, and ensure seamless execution of solution strategies for healthcare clients in Strategic, Major & Education markets. * Proven experience delivering strategic presentations and communicating effectively across all levels of a healthcare organization including stakeholders such as
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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)
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AGRER is seeking to strengthen its teams with a new Business Developer & Project Manager to identify, win, and manage development projects. * Conducting market research and commercial monitoring
AGRER is seeking to strengthen its teams with a new Business Developer & Project Manager to identify, win, and manage development projects. * Conducting market research and commercial monitoring
Doelgerichte research en het testen van nieuwe software spreken je aan, en je weet dit nuttig te gebruiken bij je job. Netwerken, SysteembeheerBachelor denkniveauMedior, Senior werkniveau2 jaar werkervaringNederlands, Engels sprekend
Doelgerichte research en het testen van nieuwe software spreken je aan, en je weet dit nuttig te gebruiken bij je job. Netwerken, SysteembeheerBachelor denkniveauMedior, Senior werkniveau2 jaar werkervaringNederlands, Engels sprekend
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. - Supported in your career by your Business Manager
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. - Supported in your career by your Business Manager
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Research and identify potential customers within relevant industries, reaching out via cold calling, email, LinkedIn, networking events, and Suivo events.
Research and identify potential customers within relevant industries, reaching out via cold calling, email, LinkedIn, networking events, and Suivo events.
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Hun expertise gaat veel verder en stelt hen in staat de industrie te ondersteunen in elke fase van ontwerp, ontwikkeling, productie en Global QA/RA Director Als Global QA/RA Director ben jij verantwoordelijk voor de aansturing en verdere ontwikkeling van de Quality Assurance afdelingen op de sites in Nederland, België, de UK en de US. Strategische en leidinggevende QA/RA-rol met internationale verantwoordelijkheid binnen een groeiende organisatie (Standplaats bespreekbaar – regelmatige aanwezigheid vereist op o.a. Hamont-Achel, Heerenveen, Rhymney en Bethlehem) * Minimaal 15 jaar relevante werkervaring binnen QA/RA in de farmaceutische industrie; * Aantoonbare ervaring in het aansturen van (internationale) QA/RA-teams
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To strengthen its global Quality organization, we are recruiting a: Global QA/RA Director * Report directly to the SVP Global Quality (dotted line to the SVP & Managing Director Clinical & Europe). Our client is a global leader in clinical and commercial packaging solutions for the pharmaceutical and biotech industry. * Be an active member of both the European Commercial Management Team and the Global Clinical Leadership Team. * Lead and coach QA Heads and sub-functions across four international sites. * Define, harmonize, and implement global quality policies, standards and procedures, aligned with cGMP, internal requirements, and client expectations. * Handle customer escalations and lead global management review processes. * Manage the quality budget and contribute to strategic planning at global level. * Additional certifications in QA/RA or GxP are a strong asset
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Oversee and coordinate major projects across the Benelux region, ensuring consistency in delivery and adherence to client-specific standards. Operating internationally, the company is recognized for its commitment to speed, excellence in execution, and rigorous delivery standards across various sectors, including strategic client projects. To oversee the delivery of high-profile projects across the Benelux region, they open a new position of * Act as the primary point of contact for strategic clients on project-related matters. * Implement and enforce Portakabin's project delivery processes, tailored to meet the elevated requirements of international clients. * Identify weaknesses in local project execution and lead improvement initiatives. * Collabor
Oversee and coordinate major projects across the Benelux region, ensuring consistency in delivery and adherence to client-specific standards. Operating internationally, the company is recognized for its commitment to speed, excellence in execution, and rigorous delivery standards across various sectors, including strategic client projects. To oversee the delivery of high-profile projects across the Benelux region, they open a new position of * Act as the primary point of contact for strategic clients on project-related matters. * Implement and enforce Portakabin's project delivery processes, tailored to meet the elevated requirements of international clients. * Identify weaknesses in local project execution and lead improvement initiatives. * Collabor
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Join us as Head of Technical Operations – Clinical Pharmacology Unit (Antwerpen)
Join us as Head of Technical Operations – Clinical Pharmacology Unit (Antwerpen)
SGS Group Belgium
Edegem
SGS is seeking a dynamic Head of Technical Operations (HTO) to lead and elevate our Clinical Pharmacology Unit (CPU) in Antwerpen. This is a high-impact role at the heart of early-phase clinical trials, where your expertise will shape the future of clinical operations and drive innovation. * Team leadership: Inspire and mentor technical operations teams, fostering collaboration and continuous development. * Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Quality assurance: Uphold SGS standards, GCP/GLP compliance, and confidentiality across all operations. At SGS, you'll be part of a global leader in clinical resea
SGS is seeking a dynamic Head of Technical Operations (HTO) to lead and elevate our Clinical Pharmacology Unit (CPU) in Antwerpen. This is a high-impact role at the heart of early-phase clinical trials, where your expertise will shape the future of clinical operations and drive innovation. * Team leadership: Inspire and mentor technical operations teams, fostering collaboration and continuous development. * Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Quality assurance: Uphold SGS standards, GCP/GLP compliance, and confidentiality across all operations. At SGS, you'll be part of a global leader in clinical resea
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