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                          51 results for Clinical Monitor jobs in Sint Agatha Berchem within a 30 km radius

                          Medical Monitor (Gastroenterology)

                          Psi Cro Belgium BV
                          Leuven
                          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
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                          BUSINESS DEVELOPMENT MANAGER, PHARMA, BIOANALYSIS DIVISION

                          SGS Group Belgium
                          Wavre
                          Easy Apply
                          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
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                          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
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                          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
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                          You closely monitor market developments related to planning needs and practices, and translate these into opportunities for Vinçotte. You develop and monitor cross-divisional capacity planning. * You create dashboards to monitor relevant KPIs and, based on these, provide recommendations to the Workforce Planning Director. * You closely monitor KPIs (e.g., timelines, volumes). * You monitor your department's financial results, identify deviations, and make adjustments as needed to achieve objectives. * You allocate budgets and resources to different teams and projects—both personnel and materials—and closely monitor their use.
                          You closely monitor market developments related to planning needs and practices, and translate these into opportunities for Vinçotte. You develop and monitor cross-divisional capacity planning. * You create dashboards to monitor relevant KPIs and, based on these, provide recommendations to the Workforce Planning Director. * You closely monitor KPIs (e.g., timelines, volumes). * You monitor your department's financial results, identify deviations, and make adjustments as needed to achieve objectives. * You allocate budgets and resources to different teams and projects—both personnel and materials—and closely monitor their use.
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                          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.
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                          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 ;
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                          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
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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.
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                          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

                          How many Clinical Monitor jobs are there in Sint Agatha Berchem?
                          There are 51 Clinical Monitor jobs within 20 miles of Sint Agatha Berchem available on StepStone right now.

                          What other similar jobs are there to Clinical Monitor jobs in Sint Agatha Berchem?
                          As well as Clinical Monitor jobs in Sint Agatha Berchem, you can find IT, Communication, Coordination, amongst many others.

                          Which skills are beneficial for Clinical Monitor jobs in Sint Agatha Berchem?
                          The following skills are useful for Clinical Monitor jobs in Sint Agatha Berchem: Communication, Coordination, Proactivity, Business, Organization Skills.

                          Which industry do Clinical Monitor jobs in Sint Agatha Berchem belong to?
                          Clinical Monitor jobs in Sint Agatha Berchem are part of the Science industry.