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62 resultaten voor Clinical research associate in Waver binnen een straal van 30 km
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Grâce à des infrastructures de pointe et une approche centrée sur le patient, le Clinical Trials Center contribue activement à la mission de l'Institut Jules Bordet : offrir à chaque patient l'accès aux traitements les plus innovants et participer au développement de la médecine de demain.
Grâce à des infrastructures de pointe et une approche centrée sur le patient, le Clinical Trials Center contribue activement à la mission de l'Institut Jules Bordet : offrir à chaque patient l'accès aux traitements les plus innovants et participer au développement de la médecine de demain.
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported ...
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-being. PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. * Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported ...
We hebben je zoekopdracht uitgebreid met 60 gelijkaardige vacatures.
Are you persuasive, analytical and eager to work with capital markets as our Investor Relations Analyst / Associate in Brussels, Belgium? The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. As our Investor Relations Analyst / Associate, you will be a key contributor to the Investor Relations team and the broader Group Finance & Administration ...
Are you persuasive, analytical and eager to work with capital markets as our Investor Relations Analyst / Associate in Brussels, Belgium? The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. As our Investor Relations Analyst / Associate, you will be a key contributor to the Investor Relations team and the broader Group Finance & Administration ...
The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. * Support the setup of the process transformation project;define the objective, list of deliverables, and associated timeline with the process owners and key users from the business. * Deploy the new process and associated tools;define and run the change management & communication plan; train the , etc.
The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. * Support the setup of the process transformation project;define the objective, list of deliverables, and associated timeline with the process owners and key users from the business. * Deploy the new process and associated tools;define and run the change management & communication plan; train the , etc.
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Located in Brussels (Machelen), our office brings together the European Technology Centre (ETC), a tech center for research and development and key business functions that drive ExxonMobil's operations across EMEAF. To support the growth of our Polymers and Performance Liquids businesses, we are looking for Research Technicians to join our Lab Operations Team.
Located in Brussels (Machelen), our office brings together the European Technology Centre (ETC), a tech center for research and development and key business functions that drive ExxonMobil's operations across EMEAF. To support the growth of our Polymers and Performance Liquids businesses, we are looking for Research Technicians to join our Lab Operations Team.
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Sander Brussels * Brussel * Freelance, Vast contract, onbepaalde tijd * Voltijds - Our client is a leading Belgian law firm with an international reach, looking to strengthen its Corporate M&A practice. Why apply? You'll join a top-tier, people-oriented law firm known for its deep expertise in tax-driven transactions, working on complex Belgian and cross-border deals. Expect high-quality files, close client exposure, and structured training within a collaborative and entrepreneurial environment. Your duties and responsibilities * Advising on M&A and Equity transactions, from structuring to post-acquisition * Assisting with tax due diligence (buy-side & sell-side) * Supporting the structuring of investment vehicles, VC & PE funds * Working on management incentive plans and equity-based schemes * Collaborating with international on cross-border transactions
Sander Brussels * Brussel * Freelance, Vast contract, onbepaalde tijd * Voltijds - Our client is a leading Belgian law firm with an international reach, looking to strengthen its Corporate M&A practice. Why apply? You'll join a top-tier, people-oriented law firm known for its deep expertise in tax-driven transactions, working on complex Belgian and cross-border deals. Expect high-quality files, close client exposure, and structured training within a collaborative and entrepreneurial environment. Your duties and responsibilities * Advising on M&A and Equity transactions, from structuring to post-acquisition * Assisting with tax due diligence (buy-side & sell-side) * Supporting the structuring of investment vehicles, VC & PE funds * Working on management incentive plans and equity-based schemes * Collaborating with international on cross-border transactions
Our client is a leading independent Belgian law firm advising major national and international , and is looking for a driven Employment Law Associate.
Our client is a leading independent Belgian law firm advising major national and international , and is looking for a driven Employment Law Associate.
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Je geeft advies over de implementatie van UX Research Methods en over de uit te voeren tests om het gedrag van de gebruikers te analyseren en te voorspellen.
Je geeft advies over de implementatie van UX Research Methods en over de uit te voeren tests om het gedrag van de gebruikers te analyseren en te voorspellen.
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Ensure appropriate documentation (URS, validation packages, data flows) is in place for external systems supporting clinical studies and activities. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle. * Assess and document Data Integrity risks associated with externally operated systems and the interfaces linking them to internal systems, ensuring that controls are in place to protect data reliability, and traceability. * Solid knowledge of GLP, GCP, GVP and GRA regulatory frameworks and associated expectations for computerized systems (e.g., OECD GLP, ICH E6(R3), EU GVP Module I/IX).
Ensure appropriate documentation (URS, validation packages, data flows) is in place for external systems supporting clinical studies and activities. * Work with Computer System QA team and Clinical Operations to ensure that DI controls (including ALCOA+ principles, metadata management, audit trails, system-to-system data transfer checks, and dataflow mapping) are embedded across the full data lifecycle. * Assess and document Data Integrity risks associated with externally operated systems and the interfaces linking them to internal systems, ensuring that controls are in place to protect data reliability, and traceability. * Solid knowledge of GLP, GCP, GVP and GRA regulatory frameworks and associated expectations for computerized systems (e.g., OECD GLP, ICH E6(R3), EU GVP Module I/IX).
Preferable 5 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 3 years in the research, clinical development or Pharmacovigilance domain.
Preferable 5 years of experience working in the (bio)pharmaceutical industry preferred, with a minimum of 3 years in the research, clinical development or Pharmacovigilance domain.
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Voorbereiden, structuren en analyseren van investeringsdossiers, ondersteund door grondige markt -en deskresearch.
Voorbereiden, structuren en analyseren van investeringsdossiers, ondersteund door grondige markt -en deskresearch.
NIEUW
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Perform analyses of raw materials, intermediate products, in bulk or packaged finished products in accordance with work instructions and established procedures (stabilities, in-process control, clinical release, investigation, ...). * Ensure stability analyses and clinical release for clinical phases I and II, as well as any analyses in support to process understanding (IPC test, forced degradation study, multimedia dissolution, ...) * Monitor the documentation associated with the analytical laboratory activities by mastering the computer softwares in use at the laboratory (eg Mikado, GLIMS, e-noval, TrackWise, ...).
Perform analyses of raw materials, intermediate products, in bulk or packaged finished products in accordance with work instructions and established procedures (stabilities, in-process control, clinical release, investigation, ...). * Ensure stability analyses and clinical release for clinical phases I and II, as well as any analyses in support to process understanding (IPC test, forced degradation study, multimedia dissolution, ...) * Monitor the documentation associated with the analytical laboratory activities by mastering the computer softwares in use at the laboratory (eg Mikado, GLIMS, e-noval, TrackWise, ...).
Strong GCP background + clinical trial management understanding.
Strong GCP background + clinical trial management understanding.
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Pfizer has four offices in Belgium with which it supports its Belgian and international activities: 1) Anderlecht, where the Pfizer Clinical Research Unit is located. This is a fully equipped phase 1 research center. With that of New Haven (US), it is one of two Phase 1 Pfizer research centers in the world, 2)Elsene, the Belgian headquarters, 3)Puurs, Pfizer's production and packaging site, and 4) Zaventem, the international Pfizer's Logistics Center.
Pfizer has four offices in Belgium with which it supports its Belgian and international activities: 1) Anderlecht, where the Pfizer Clinical Research Unit is located. This is a fully equipped phase 1 research center. With that of New Haven (US), it is one of two Phase 1 Pfizer research centers in the world, 2)Elsene, the Belgian headquarters, 3)Puurs, Pfizer's production and packaging site, and 4) Zaventem, the international Pfizer's Logistics Center.
You conduct studies on electrical installations (low voltage and medium voltage) and associated low-current systems (security systems, alarms, structured cabling…).
You conduct studies on electrical installations (low voltage and medium voltage) and associated low-current systems (security systems, alarms, structured cabling…).
NIEUW
Conduct in vitro experiments to identify potential liabilities in pre-clinical drug development
Conduct in vitro experiments to identify potential liabilities in pre-clinical drug development
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Snel solliciteren
Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Bioanalysis Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business;
Actively prospecting new customers and new business opportunities worldwide and develop new opportunities with existing clients on Preclinical (GLP) and Clinical (GCLP) Bioanalytical projects. with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Bioanalysis Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business;
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We reinvest our profits into research and development, helping to lower the cost of participating in sport.
We reinvest our profits into research and development, helping to lower the cost of participating in sport.
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Je evalueert werkmethodes, investeringsmaterialen en staat in voor research naar oplossingen voor schoonmaakproblemen en beheert onze interne kennisbank.
Je evalueert werkmethodes, investeringsmaterialen en staat in voor research naar oplossingen voor schoonmaakproblemen en beheert onze interne kennisbank.
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Assist with setting up security, file access and other administrative procedures associated with moves
Assist with setting up security, file access and other administrative procedures associated with moves
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Snel solliciteren
Lead Generation and Qualification: Generate leads through networking, industry events, and online research, focusing on potential clients in Belgium.
Lead Generation and Qualification: Generate leads through networking, industry events, and online research, focusing on potential clients in Belgium.
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It employs roughly 429,000 associates worldwide (as of December 31, 2023).
It employs roughly 429,000 associates worldwide (as of December 31, 2023).
NIEUW
Research and writing: support campaigning and senior staff with relevant research, by editing documents or developing support materials (e.g., briefing documents, conference support, decks, talking points).
Research and writing: support campaigning and senior staff with relevant research, by editing documents or developing support materials (e.g., briefing documents, conference support, decks, talking points).
and risk management strategies associated with global value chains
and risk management strategies associated with global value chains
NIEUW
and risk management strategies associated with global value chains
and risk management strategies associated with global value chains
NIEUW