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82 results for Clinical Monitor jobs in Saint Gilles within a 30 km radius
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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-. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and , while always focusing on patients' safety and well-. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry. * Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations * Review and analysis of clinical data to ensure the safety of study participants in clinical studies
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
No match yet? There are 79 more jobs that could match your search
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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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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; * Establish, monitor and coordinate timely action plans, taking into consideration positive and negative deviations from target
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; * Establish, monitor and coordinate timely action plans, taking into consideration positive and negative deviations from target
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. * Monitor and follow-up on intercompany payables.
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. * Monitor and follow-up on intercompany payables.
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. * Monitor and follow-up on intercompany payables.
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. * Monitor and follow-up on intercompany payables.
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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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Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
Monitor HR Consulting
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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).
Strong GCP background + clinical trial management understanding.
Strong GCP background + clinical trial management understanding.
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Organize and monitor on-site security. * Monitor and approve vendor performance and invoicing.
Organize and monitor on-site security. * Monitor and approve vendor performance and invoicing.
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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
Implement or coordinate & monitor development, testing, issues/defects identification, prioritization & fixes
Implement or coordinate & monitor development, testing, issues/defects identification, prioritization & fixes
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Monitor project planning, milestones, and overall achievements.
Monitor project planning, milestones, and overall achievements.
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Monitor production batches
Monitor production batches
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Implement and monitor financial procedures, including monthly and annual closings, bank reconciliations, and reporting.
Implement and monitor financial procedures, including monthly and annual closings, bank reconciliations, and reporting.
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Monitor new sustainability regulations and translate them into clear actions
Monitor new sustainability regulations and translate them into clear actions
Monitors continuously this overall project schedule file and keeps the informed regarding the progress and alerts problems/conflicts relating to the execution of project tasks and interrelations of project activities
Monitors continuously this overall project schedule file and keeps the informed regarding the progress and alerts problems/conflicts relating to the execution of project tasks and interrelations of project activities