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43 results for Clinical Trial Liaison jobs
As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment techniques.
As a Clinical Trial Liaison, you will help clinical sites identify and recruit patients more efficiently by providing protocol‑focused support. Acting as the face of PSI on-site, you will be a key contributor to the success of our clinical trials and a trusted resource for site teams. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French * Serve as a specialized liaison to support sites with a protocol‑tailored strategy that enhances patient identification and recruitment efficiency. * Guide clinical sites in developing and implementing effective patient enrolment techniques.
No match yet? There are 42 more jobs that could match your search
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Om hun technische ondersteuning en productpositionering binnen Export verder te professionaliseren, zoeken zij een Field Trials Project Coordinator. Als Field Trials Projectmanager word jij dé inhoudelijke expert voor het trials en toegepaste proeven bij exportklanten en partners. * Ervaring met proeven, trials, data-analyse of toegepast onderzoek.
Om hun technische ondersteuning en productpositionering binnen Export verder te professionaliseren, zoeken zij een Field Trials Project Coordinator. Als Field Trials Projectmanager word jij dé inhoudelijke expert voor het trials en toegepaste proeven bij exportklanten en partners. * Ervaring met proeven, trials, data-analyse of toegepast onderzoek.
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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.
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The Clinical Diabetes Sales Specialist is directly responsible for the promotion and sale of Tandem Diabetes products and clinical services within the assigned territory. He / She is expected to plan and ensure achievement of sales goals through clinical acceptance of Tandem products' insulin pump therapy. * Develop and execute effective strategies to address clinical needs, drive adoption of Tandem Diabetes products and services, and retain existing customer relationships. * Serve as a clinical and educational leader within the territory, with a strong focus on Type 1 diabetes management and insulin pump therapy. * Create value for by clearly differentiating Tandem's technology, services, and clinical advantages, particularly versus legacy pump systems, while effectively communicating Tandem's unique market position and competitive strengths.
The Clinical Diabetes Sales Specialist is directly responsible for the promotion and sale of Tandem Diabetes products and clinical services within the assigned territory. He / She is expected to plan and ensure achievement of sales goals through clinical acceptance of Tandem products' insulin pump therapy. * Develop and execute effective strategies to address clinical needs, drive adoption of Tandem Diabetes products and services, and retain existing customer relationships. * Serve as a clinical and educational leader within the territory, with a strong focus on Type 1 diabetes management and insulin pump therapy. * Create value for by clearly differentiating Tandem's technology, services, and clinical advantages, particularly versus legacy pump systems, while effectively communicating Tandem's unique market position and competitive strengths.
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We're expanding our Clinical Research business and are looking for a passionate and strategic Business Development Manager to drive growth across Western Europe. You'll build strong relationships, close impactful deals, and help shape the future of clinical research at SGS. * Solid experience in Clinical Research, CRO, or related fields. * Deep understanding of the clinical drug development process.
We're expanding our Clinical Research business and are looking for a passionate and strategic Business Development Manager to drive growth across Western Europe. You'll build strong relationships, close impactful deals, and help shape the future of clinical research at SGS. * Solid experience in Clinical Research, CRO, or related fields. * Deep understanding of the clinical drug development process.
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To support our continued growth, we're looking for a passionate and strategic Key Account Manager to join our Clinical Research team. Your Role: Key Account Manager – Clinical Research - You'll drive growth, build long-term relationships, and act as the vital link between our clients and SGS's global Clinical Research Organization. * Proven experience in Key Account Management, sales, or client relationship roles—ideally within a CRO or Clinical Research setting.
To support our continued growth, we're looking for a passionate and strategic Key Account Manager to join our Clinical Research team. Your Role: Key Account Manager – Clinical Research - You'll drive growth, build long-term relationships, and act as the vital link between our clients and SGS's global Clinical Research Organization. * Proven experience in Key Account Management, sales, or client relationship roles—ideally within a CRO or Clinical Research setting.
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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
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 - o Strong clinical trial knowledge and strategic thinking - Are you a strategic leader with a passion for clinical research and operational excellence? SGS is seeking a dynamic Head of Technical Operations (HTO) to lead and elevate our Clinical Pharmacology Unit (CPU) in Antwerpen. * Clinical Floor Experts * Education: Higher degree in Clinical Activities or Life Sciences * 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 ...
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 - o Strong clinical trial knowledge and strategic thinking - Are you a strategic leader with a passion for clinical research and operational excellence? SGS is seeking a dynamic Head of Technical Operations (HTO) to lead and elevate our Clinical Pharmacology Unit (CPU) in Antwerpen. * Clinical Floor Experts * Education: Higher degree in Clinical Activities or Life Sciences * 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 ...
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Strong GCP background + clinical trial management understanding.
Strong GCP background + clinical trial management understanding.
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Location: SGS – Clinical Research Division - Ready to shape the future of clinical research? We're looking for a passionate and driven Business Development Manager to lead the growth of our Biometrics services within the Clinical Research space. As our Business Development Manager Biometrics, you'll be the strategic force behind expanding our biometrics services (including data management and biostatistics) in the clinical research sector. * Solid understanding of clinical research, CRO operations, and biometrics (data management and/or biostatistics).
Location: SGS – Clinical Research Division - Ready to shape the future of clinical research? We're looking for a passionate and driven Business Development Manager to lead the growth of our Biometrics services within the Clinical Research space. As our Business Development Manager Biometrics, you'll be the strategic force behind expanding our biometrics services (including data management and biostatistics) in the clinical research sector. * Solid understanding of clinical research, CRO operations, and biometrics (data management and/or biostatistics).
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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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Azuro * Brussel & thuiswerk * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Introductie - Azuro is op zoek naar een Legal Advisor voor NN Insurance. Je maakt daarbij deel uit van een hecht en enthousiast team met veel expertise. Het gaat om een transversaal legal departement, dus je kan je uitleven in verschillende onderwerpen en juridische materies binnen de sector van levensverzekeringen. Over NN - NN België maakt deel uit van NN Group, een internationale verzekeringsgroep en vermogensbeheerder. De groep is actief in 11 landen en verkeert in goede financiële gezondheid. Met meer dan 600 medewerkers dragen ze in België bij tot de financiële gemoedsrust van meer dan 1,2 miljoen klanten. Ze staan ten dienste van hun klanten via hun partnernetwerk van banken en makelaars; een netwerk dat blijft groeien.
Azuro * Brussel & thuiswerk * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Introductie - Azuro is op zoek naar een Legal Advisor voor NN Insurance. Je maakt daarbij deel uit van een hecht en enthousiast team met veel expertise. Het gaat om een transversaal legal departement, dus je kan je uitleven in verschillende onderwerpen en juridische materies binnen de sector van levensverzekeringen. Over NN - NN België maakt deel uit van NN Group, een internationale verzekeringsgroep en vermogensbeheerder. De groep is actief in 11 landen en verkeert in goede financiële gezondheid. Met meer dan 600 medewerkers dragen ze in België bij tot de financiële gemoedsrust van meer dan 1,2 miljoen klanten. Ze staan ten dienste van hun klanten via hun partnernetwerk van banken en makelaars; een netwerk dat blijft groeien.
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, ...)
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, ...)
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Smals * Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Smals realiseert innovatieve ICT-projecten in e-government en e-health voor instellingen uit de sociale zekerheid en de gezondheidszorg. 'ICT for society' is voor Smals meer dan een slogan: alle projecten hebben een positieve maatschappelijke impact. Zo bouwt Smals mee aan het portaal van de sociale zekerheid en het eHealth-platform. Jouw verantwoordelijkheden - Als Infrastructure Scrum Master maak je deel uit van de afdeling IT infrastructuur en zal je één of meerdere agile teams ondersteunen. Je rapporteert aan de . In deze functie faciliteer en stimuleer je de samenwerking binnen de teams en zorg je ervoor dat Scrum-evenementen (sprint planning, reviews, retrospectives, …) correct verlopen en afgestemd zijn op de infrastructuuromgeving (incidenten, changes, ...
Smals * Brussel * Vast contract, onbepaalde tijd * Thuiswerken mogelijk, Voltijds - Solliciteer als één van de eersten - Smals realiseert innovatieve ICT-projecten in e-government en e-health voor instellingen uit de sociale zekerheid en de gezondheidszorg. 'ICT for society' is voor Smals meer dan een slogan: alle projecten hebben een positieve maatschappelijke impact. Zo bouwt Smals mee aan het portaal van de sociale zekerheid en het eHealth-platform. Jouw verantwoordelijkheden - Als Infrastructure Scrum Master maak je deel uit van de afdeling IT infrastructuur en zal je één of meerdere agile teams ondersteunen. Je rapporteert aan de . In deze functie faciliteer en stimuleer je de samenwerking binnen de teams en zorg je ervoor dat Scrum-evenementen (sprint planning, reviews, retrospectives, …) correct verlopen en afgestemd zijn op de infrastructuuromgeving (incidenten, changes, ...
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Werk je graag in een hoogtechnologische cleanroomomgeving waar trial & error, precisie en samenwerking centraal staan? * Het opzetten, uitvoeren en opvolgen van trial & error-testen op industriële testmachines in cleanroomomgeving.
Werk je graag in een hoogtechnologische cleanroomomgeving waar trial & error, precisie en samenwerking centraal staan? * Het opzetten, uitvoeren en opvolgen van trial & error-testen op industriële testmachines in cleanroomomgeving.
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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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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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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Serve as the liaison between clients and internal teams (strategy, creative, tech), ensuring clear communication and alignment.
Serve as the liaison between clients and internal teams (strategy, creative, tech), ensuring clear communication and alignment.
Je begeleidt testen, demo's en industriële trials.
Je begeleidt testen, demo's en industriële trials.
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vous assurez un rôle de liaison avec les différents départements internes ainsi qu'avec les partenaires externes (secrétariat social, assurance, SEPPT, etc.) ;
vous assurez un rôle de liaison avec les différents départements internes ainsi qu'avec les partenaires externes (secrétariat social, assurance, SEPPT, etc.) ;
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SGS Life Sciences is a leading contract research organization offering Clinical Research Drug Development and Quality Control/Laboratory Testing Services to the pharmaceutical and biopharmaceutical industry.
SGS Life Sciences is a leading contract research organization offering Clinical Research Drug Development and Quality Control/Laboratory Testing Services to the pharmaceutical and biopharmaceutical industry.
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 * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations
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 * Review and analysis of clinical data to ensure the safety of study participants in clinical trials * Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments - PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations
Fulltime contract (including evening and weekend work) - after a trial with no end date
Fulltime contract (including evening and weekend work) - after a trial with no end date
You will be responsible for the technical vision, development, and maintenance of our platform while also serving as a key liaison between business and the technical team.
You will be responsible for the technical vision, development, and maintenance of our platform while also serving as a key liaison between business and the technical team.
Business Development Manager Non-Sterile Drug Product Development and Manufacturing
Business Development Manager Non-Sterile Drug Product Development and Manufacturing
Eurofins Belgium
Ghent
We support small and major biopharmaceutical companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our facilities are perfectly designed for clinical and/or small scale commercial batches either for non-sterile or sterile dosage forms. To support our ambitious growth plan in formulation, analytical development and GMP manufacturing of clinical batches, we are today looking for a talented Business Development Manager Non-Sterile Drug Product Development and * Focusing on development projects particularly the earliest phases up to clinical development (Phase 1 to 2B) for chemical and/or biological compounds;
We support small and major biopharmaceutical companies in an innovative way to help them achieving their (pre)clinical milestones timely. Our facilities are perfectly designed for clinical and/or small scale commercial batches either for non-sterile or sterile dosage forms. To support our ambitious growth plan in formulation, analytical development and GMP manufacturing of clinical batches, we are today looking for a talented Business Development Manager Non-Sterile Drug Product Development and * Focusing on development projects particularly the earliest phases up to clinical development (Phase 1 to 2B) for chemical and/or biological compounds;
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