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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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
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. * Monitor, track, and report patient enrolment progress throughout the study lifecycle. * Advise and collaborate with site monitors on patient recruitment strategies. * 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. * Monitor, track, and report patient enrolment progress throughout the study lifecycle. * Advise and collaborate with site monitors on patient recruitment strategies. * At least 5 years of relevant clinical practice experience, including patient‑enrolment strategies for clinical trials * Full working proficiency in English, Dutch and French
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
Political, policy and regulatory analysis: monitor, analyze and report on emerging public policy issues on European sustainability and climate policy with a focus on AI & energy, datacenter sustainability, energy grids, circular economy and carbon removals.
Political, policy and regulatory analysis: monitor, analyze and report on emerging public policy issues on European sustainability and climate policy with a focus on AI & energy, datacenter sustainability, energy grids, circular economy and carbon removals.
Project Management: Actively participate in project management, monitor progress, coordinate actions with and , while respecting deadlines and budgets ;
Project Management: Actively participate in project management, monitor progress, coordinate actions with and , while respecting deadlines and budgets ;
Monitor stock performance, times, and service levels - Define, monitor, and analyze key performance indicators (KPIs) including service level, capacity calculations, delivery times, logistics costs, inventory turnover, and stock health
Monitor stock performance, times, and service levels - Define, monitor, and analyze key performance indicators (KPIs) including service level, capacity calculations, delivery times, logistics costs, inventory turnover, and stock health
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.
Financial Control: You validate invoices and monitor the transport budget with an analytical and sharp eye. * Performance Management: You monitor 'Carrier on Time' and NPS (Post-Delivery Satisfaction), adjusting where necessary.
Financial Control: You validate invoices and monitor the transport budget with an analytical and sharp eye. * Performance Management: You monitor 'Carrier on Time' and NPS (Post-Delivery Satisfaction), adjusting where necessary.
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.
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.
Define and monitor data-related KPIs to ensure the delivery of high-quality, reliable * Implement tools and systems to monitor and report on operational performance.
Define and monitor data-related KPIs to ensure the delivery of high-quality, reliable * Implement tools and systems to monitor and report on operational performance.
What is the average salary for Clinical Monitor in Sint Agatha Berchem?
Average salary per year
42.200 €
The average salary for a Clinical Monitor in Sint Agatha Berchem is 42.200 €. Clinical Monitor in Sint Agatha Berchem salaries range from 35.200 € to 51.200 €.
Frequently Asked Questions
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