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26 results for Clinical Reasoning jobs in Machelen, Vlaams Brabant within a 30 km radius
Woonzorgnet-Dijleland VZW * HULDENBERG - Solliciteer als één van de eersten - expert in warme zorg en coördinatie - Je bewaakt de kwaliteit van zorg voor bewoners met complexe, vaak multipathologische zorgvragen. Je voert gespecialiseerde verpleegtechnische handelingen uit (zoals wondzorg, palliatieve sedatie …). Je past klinisch redeneren toe en maakt onderbouwde keuzes in zorg. Je werkt nauw samen met , , en familie – en coördineert de multidisciplinaire aanpak. Je bent een coach voor en durft verantwoordelijkheid nemen in gevarieerde zorgsituaties. Je zorgt mee voor een klimaat van continu leren, reflecteren en verbeteren. Jouw profiel - Je hebt een diploma als verpleegkundige (bachelor of HBO5). Je hebt een passie voor ouderenzorg. Je denkt kritisch en klinisch. Je beslissingen zijn doordacht, onderbouwd en in het belang van de bewoner. Je communiceert helder en professioneel.
Woonzorgnet-Dijleland VZW * HULDENBERG - Solliciteer als één van de eersten - expert in warme zorg en coördinatie - Je bewaakt de kwaliteit van zorg voor bewoners met complexe, vaak multipathologische zorgvragen. Je voert gespecialiseerde verpleegtechnische handelingen uit (zoals wondzorg, palliatieve sedatie …). Je past klinisch redeneren toe en maakt onderbouwde keuzes in zorg. Je werkt nauw samen met , , en familie – en coördineert de multidisciplinaire aanpak. Je bent een coach voor en durft verantwoordelijkheid nemen in gevarieerde zorgsituaties. Je zorgt mee voor een klimaat van continu leren, reflecteren en verbeteren. Jouw profiel - Je hebt een diploma als verpleegkundige (bachelor of HBO5). Je hebt een passie voor ouderenzorg. Je denkt kritisch en klinisch. Je beslissingen zijn doordacht, onderbouwd en in het belang van de bewoner. Je communiceert helder en professioneel.
No match yet? There are 25 more jobs that could match your search
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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
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. 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 * Experience: 5–8 years in clinical research, ideally with Phase 1 exposure; 3–5 years in team leadership - o Strong clinical trial knowledge and strategic thinking - At SGS, you'll be part of a global leader in clinical research, working in a collaborative ...
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. 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 * Experience: 5–8 years in clinical research, ideally with Phase 1 exposure; 3–5 years in team leadership - o Strong clinical trial knowledge and strategic thinking - At SGS, you'll be part of a global leader in clinical research, working in a collaborative ...
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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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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.
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.
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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Strong GCP background + clinical trial management understanding.
Strong GCP background + clinical trial management understanding.
Your analytical skills and logical reasoning are your key assets.
Your analytical skills and logical reasoning are your key assets.
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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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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.
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.
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. * Guide clinical sites in developing and implementing effective patient enrolment techniques. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French
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. * Guide clinical sites in developing and implementing effective patient enrolment techniques. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French
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Using a Python-native stack (Streamlit, Boto3, LangChain), you will develop a decoupled back-end capable of sophisticated reasoning, while simultaneously building the CI/CD pipelines and Infrastructure as Code (IaC) required to deploy this solution at scale.
Using a Python-native stack (Streamlit, Boto3, LangChain), you will develop a decoupled back-end capable of sophisticated reasoning, while simultaneously building the CI/CD pipelines and Infrastructure as Code (IaC) required to deploy this solution at scale.
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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. * 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 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 , while always focusing on patients' safety and well-being. * 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 trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
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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.
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.
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Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
Ensure compliance with regulatory and quality standards relevant to multiple geographies, products and industries including biopharmaceuticals, clinical diagnostics, and direct to consumer sales.
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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.
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.
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.
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.
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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.
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.
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.