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8 results for Clinical Research Associate Senior jobs in Baarle Hertog 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 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
No match yet? There are 7 more jobs that could match your search
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? 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 o
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? 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 o
The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. * 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 will engage with key , vendors, and teams/peers responsible for training creation, facilitation, and delivery. * Keeps abreast of training and development research within/out of industry, new materials, methodologies. * Serves as a key contact for the GCO Organization for training and le
The Senior Manager is responsible for deploying organizational training strategy and delivery across clinical trial and role-based training programs. * 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 will engage with key , vendors, and teams/peers responsible for training creation, facilitation, and delivery. * Keeps abreast of training and development research within/out of industry, new materials, methodologies. * Serves as a key contact for the GCO Organization for training and le
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
The Senior Director MSAT SO&P is accountable for ideating, shaping, driving and optimizing business and technical processes, with associated tools that are essential to the business strategy execution within the ever-changing business landscape. We are searching for the best talent for Senior Director MSAT Strategic Operations & Packaging role - The Senior Director MSAT SO&P drives a culture of agility, innovation, technical excellence, business acumen and harmonized ways of working across MSAT. The leader will communicate performance, progress, challenges, and achievements to stakeholders at all levels, including senior management. Identify risks associated and develop proactive mitigation strategies. * Demonstrated senior level management overseeing
The Senior Director MSAT SO&P is accountable for ideating, shaping, driving and optimizing business and technical processes, with associated tools that are essential to the business strategy execution within the ever-changing business landscape. We are searching for the best talent for Senior Director MSAT Strategic Operations & Packaging role - The Senior Director MSAT SO&P drives a culture of agility, innovation, technical excellence, business acumen and harmonized ways of working across MSAT. The leader will communicate performance, progress, challenges, and achievements to stakeholders at all levels, including senior management. Identify risks associated and develop proactive mitigation strategies. * Demonstrated senior level management overseeing
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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).
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.
9 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. * 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.
Als Associate Partner ben jij de verbindende schakel tussen onze klanten, hun projecten en ons netwerk van HR-coaches en . * Partnerschap : je combineert je rol als Associate Partner met je eigen HR-projecten.
Als Associate Partner ben jij de verbindende schakel tussen onze klanten, hun projecten en ons netwerk van HR-coaches en . * Partnerschap : je combineert je rol als Associate Partner met je eigen HR-projecten.
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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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The senior Business Development & Partnership Manager is a key driver within the sales team. * Propose associated marketing and distribution strategies to transform prospects into new business.
The senior Business Development & Partnership Manager is a key driver within the sales team. * Propose associated marketing and distribution strategies to transform prospects into new business.
Conducting market research and commercial monitoring
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
Together with a team of senior associates, you will work on various client assignments related to the employment of in Belgium.
Together with a team of senior associates, you will work on various client assignments related to the employment of in Belgium.
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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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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Europ Assistance Belgium
Brussel
Partially remote
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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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