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                          101 results for Clinical Research Associate jobs

                          Clinical Research Associate (H/F/X) - CDI- 38h/semaine - Bordet

                          H.U.B.
                          Bruxelles
                          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.
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                          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 ...
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                          No match yet? There are 99 more jobs that could match your search

                          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 ...
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                          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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                          Are you a strategic leader with a passion for clinical research and operational excellence? * Experience: 5–8 years in clinical research, ideally with Phase 1 exposure; 3–5 years in team leadership - At SGS, you'll be part of a global leader in clinical research, working in a collaborative and innovative environment. 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. * Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Clinical Trial Staff Planners * Clinical Floor Experts * Education: Higher degree in Clinical Activities or Life Sciences
                          Are you a strategic leader with a passion for clinical research and operational excellence? * Experience: 5–8 years in clinical research, ideally with Phase 1 exposure; 3–5 years in team leadership - At SGS, you'll be part of a global leader in clinical research, working in a collaborative and innovative environment. 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. * Leading clinical trial operations: Oversee multidisciplinary study execution, ensuring quality, timeliness, and sponsor satisfaction. * Clinical Trial Staff Planners * Clinical Floor Experts * Education: Higher degree in Clinical Activities or Life Sciences
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                          Research Lab Technician

                          Exxon Mobil Corporation
                          Machelen, Brussels,Belgium, BRU, BE
                          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 * Brussels * Freelance, Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - 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
                          Sander Brussels * Brussels * Freelance, Vast contract, onbepaalde tijd * Voltijds - Solliciteer als één van de eersten - 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
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                          Our partner is looking for a Quality Project Associate to join its team. The Quality Project Associating services focus on quality oversight and project support, delivering essential quality oversight and comprehensive project support for pharmaceutical processes and products within the company Belgian sites, specifically the aseptic manufacturing plant.
                          Our partner is looking for a Quality Project Associate to join its team. The Quality Project Associating services focus on quality oversight and project support, delivering essential quality oversight and comprehensive project support for pharmaceutical processes and products within the company Belgian sites, specifically the aseptic manufacturing plant.
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                          Jobstudenten klinisch onderzoek

                          SGS Group Belgium
                          Edegem
                          Easy Apply
                          Eind vorig jaar werd het nieuwe, hypermoderne centrum voor klinisch onderzoek, de SGS Clinical Pharmacology Unit, geopend te Edegem op de campus van het Universitair Ziekenhuis Antwerpen.
                          Eind vorig jaar werd het nieuwe, hypermoderne centrum voor klinisch onderzoek, de SGS Clinical Pharmacology Unit, geopend te Edegem op de campus van het Universitair Ziekenhuis Antwerpen.
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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).
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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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                          Associate's or Bachelor's degree in Microbiology, Biology, or a related scientific discipline.
                          Associate's or Bachelor's degree in Microbiology, Biology, or a related scientific discipline.
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                          TG-Packaging BV * Beveren-Kruibeke-Zwijndrecht - Solliciteer als één van de eersten - Introductie - TG-Packaging is een toonaangevend bedrijf gespecialiseerd in de verpakkingsindustrie. We bouwen industriële verpakkingsmachines voor klanten over heel de wereld. Denk maar aan koekjes, wafels of Pokémon kaarten, onze machines verpakken het allemaal. Job omschrijving * Je gaat concepten van klanten vertalen naar een modulair systeem * Je maakt 3D ontwerpen van de verpakkingsmachines * Je zorgt voor berekeningen en onderzoekt wat van toepassing is op jouw huidige project * Je past technische dossiers aan waar nodig * Je ontvangt en maakt de afweging tussen prijs en kwaliteit - Jouw profiel * Je hebt ervaring met 3D tekenen, kennis van een tekenprogramma zoals bijvoorbeeld Solidworks is een plus * Je bent vlot met de computer, office,...
                          TG-Packaging BV * Beveren-Kruibeke-Zwijndrecht - Solliciteer als één van de eersten - Introductie - TG-Packaging is een toonaangevend bedrijf gespecialiseerd in de verpakkingsindustrie. We bouwen industriële verpakkingsmachines voor klanten over heel de wereld. Denk maar aan koekjes, wafels of Pokémon kaarten, onze machines verpakken het allemaal. Job omschrijving * Je gaat concepten van klanten vertalen naar een modulair systeem * Je maakt 3D ontwerpen van de verpakkingsmachines * Je zorgt voor berekeningen en onderzoekt wat van toepassing is op jouw huidige project * Je past technische dossiers aan waar nodig * Je ontvangt en maakt de afweging tussen prijs en kwaliteit - Jouw profiel * Je hebt ervaring met 3D tekenen, kennis van een tekenprogramma zoals bijvoorbeeld Solidworks is een plus * Je bent vlot met de computer, office,...
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                          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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                          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, ...).
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                          We develop and manufacture diagnostic tests at our site in Ghent, as well as in Tokyo, after which they are sold worldwide by our commercial teams to hospitals and clinical laboratories. Join our team as an In-House Legal Counsel and step into the challenging environment of the diagnostic devices sector where you'll learn fast and make real impact across the entire value chain — from R&D and clinical innovation to marketing and sales. * Draft, review, and negotiate commercial, clinical and R&D-related agreements. keywords: junior legal counsel, junior juridisch adviseur, in-house legal counsel, legal advisor, juridisch adviseur, corporate legal counsel, bedrijfsjurist, juridisch medewerker, junior corporate counsel, assistant legal counsel, legal officer, juridisch specialist, in-house counsel, legal associate, bedrijfsjuridisch adviseur, contract manager, legal consultant, zwijnaarde, gent
                          We develop and manufacture diagnostic tests at our site in Ghent, as well as in Tokyo, after which they are sold worldwide by our commercial teams to hospitals and clinical laboratories. Join our team as an In-House Legal Counsel and step into the challenging environment of the diagnostic devices sector where you'll learn fast and make real impact across the entire value chain — from R&D and clinical innovation to marketing and sales. * Draft, review, and negotiate commercial, clinical and R&D-related agreements. keywords: junior legal counsel, junior juridisch adviseur, in-house legal counsel, legal advisor, juridisch adviseur, corporate legal counsel, bedrijfsjurist, juridisch medewerker, junior corporate counsel, assistant legal counsel, legal officer, juridisch specialist, in-house counsel, legal associate, bedrijfsjuridisch adviseur, contract manager, legal consultant, zwijnaarde, gent
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                          Contec * Antwerp * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Introductie - Dat automatisatie de toekomst is, hoeven we je vast niet te vertellen. Bij Contec maken we er dan ook onze missie van om industriële processen future proof te maken. We zijn in volle groei en daarom ook continu op zoek naar nieuwe collega's. Ben jij er klaar voor om samen met ons aan de factory of the future te bouwen? Dat kan! Voor ons Manufacturing Control team, dat zich bezighoudt met PLC-programmatie en visualisatie, zijn we momenteel op zoek naar een Automation Engineer met een passie voor automatisatie. Taken - Projecten van A-Z, dat doen we zo! Bij Contec realiseren we projecten van A tot Z. Als Automation Engineer ben je niet alleen verantwoordelijk voor het technische aspect: ook de tussentijdse communicatie met de klant en de start-up van een grote range aan projecten behoren ...
                          Contec * Antwerp * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Introductie - Dat automatisatie de toekomst is, hoeven we je vast niet te vertellen. Bij Contec maken we er dan ook onze missie van om industriële processen future proof te maken. We zijn in volle groei en daarom ook continu op zoek naar nieuwe collega's. Ben jij er klaar voor om samen met ons aan de factory of the future te bouwen? Dat kan! Voor ons Manufacturing Control team, dat zich bezighoudt met PLC-programmatie en visualisatie, zijn we momenteel op zoek naar een Automation Engineer met een passie voor automatisatie. Taken - Projecten van A-Z, dat doen we zo! Bij Contec realiseren we projecten van A tot Z. Als Automation Engineer ben je niet alleen verantwoordelijk voor het technische aspect: ook de tussentijdse communicatie met de klant en de start-up van een grote range aan projecten behoren ...
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                          Contec * Antwerp * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Introductie - Dat automatisatie de toekomst is, hoeven we je vast niet te vertellen. Bij Contec maken we er dan ook onze missie van om industriële processen future proof te maken. We zijn in volle groei en daarom ook continu op zoek naar nieuwe collega's. Ben jij er klaar voor om samen met ons aan de factory of the future te bouwen? Dat kan! Voor ons E&I team, dat zich voornamelijk bezighoudt met het elektrisch ontwerp van installaties, zijn we momenteel op zoek naar een Electrical Engineer met een passie voor elektriciteit en engineering. Taken - Projecten van A-Z, dat doen we zo! Bij Contec realiseren we projecten van A tot Z. Als E&I engineer word je mee ingezet op onze lopende projecten. * Uitwerken van schema's, kastlayouts en componentselecties.
                          Contec * Antwerp * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Introductie - Dat automatisatie de toekomst is, hoeven we je vast niet te vertellen. Bij Contec maken we er dan ook onze missie van om industriële processen future proof te maken. We zijn in volle groei en daarom ook continu op zoek naar nieuwe collega's. Ben jij er klaar voor om samen met ons aan de factory of the future te bouwen? Dat kan! Voor ons E&I team, dat zich voornamelijk bezighoudt met het elektrisch ontwerp van installaties, zijn we momenteel op zoek naar een Electrical Engineer met een passie voor elektriciteit en engineering. Taken - Projecten van A-Z, dat doen we zo! Bij Contec realiseren we projecten van A tot Z. Als E&I engineer word je mee ingezet op onze lopende projecten. * Uitwerken van schema's, kastlayouts en componentselecties.
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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.
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                          What is the average salary for Clinical Research Associate?

                          Average salary per year
                          40.700 €

                          The average salary for a Clinical Research Associate is 40.700 €. Clinical Research Associate salaries range from 34.600 € to 50.200 €.

                          Frequently Asked Questions

                          How many Clinical Research Associate jobs are available on StepStone?
                          There are 101 Clinical Research Associate jobs available on StepStone right now.

                          What other similar jobs are there to Clinical Research Associate jobs?
                          As well as Clinical Research Associate jobs, you can find IT, Communication, Engineering, amongst many others.

                          How many temporary and part-time Clinical Research Associate jobs are available?
                          There are 0 temporary Clinical Research Associate jobs and 4 part-time Clinical Research Associate jobs available at the moment.

                          Which places are popular for Clinical Research Associate jobs?
                          People who are interested in Clinical Research Associate jobs prefer to look in Brussels, Antwerp, Ghent.

                          Which industry do Clinical Research Associate jobs belong to?
                          Clinical Research Associate jobs are part of the Science industry.

                          Which skills are beneficial for Clinical Research Associate jobs?
                          The following skills are useful for Clinical Research Associate jobs: Communication, Engineering, Business, Design, Problem Management.