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                          14 results for Clinical Monitor jobs in Ganshoren within a 30 km radius

                          Clinical Research Associate (H/F/X) - CDI- 38h/semaine - Bordet

                          H.U.B.
                          Bruxelles
                          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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                          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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                          No match yet? There are 12 more jobs that could match your search

                          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. * Monitor and improve customer satisfaction, resolve issues, and gather feedback.
                          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. * Monitor and improve customer satisfaction, resolve issues, and gather feedback.
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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. * Help monitor performance and follow up on quality or delivery issues.
                          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. * Help monitor performance and follow up on quality or delivery issues.
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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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                          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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                          Business IT manager – CSV

                          SGS Group Belgium
                          Wavre
                          Easy Apply
                          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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                          Monitor and analyse evolving European and Belgian regulations, including publications by local financial authorities, to assess impact and risks for the investment department
                          Monitor and analyse evolving European and Belgian regulations, including publications by local financial authorities, to assess impact and risks for the investment department
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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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                          Manage and monitor all installed systems and infrastructure * Monitor and test application performance for potential bottlenecks, identify possible solutions, and work with to implement those fixes
                          Manage and monitor all installed systems and infrastructure * Monitor and test application performance for potential bottlenecks, identify possible solutions, and work with to implement those fixes
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                          Als Business Continuity Manager ben je verantwoordelijk voor het ontwikkelen, implementeren en borgen van de strategie op het gebied van bedrijfscontinuïteit en veerkracht binnen een snel veranderende IT-omgeving. • Je ontwikkelt en stuurt de enterprise-wide Business Continuity Management (BCM) strategie aan. • Minimaal 7 jaar ervaring in Business Continuity Management of IT Risk Management. • Je coördineert Business Impact Analyses (BIA's) en risico-assessments en baseert er de Business Continuityplannen op. • Een achtergrond in IT, Security, Risk of Business Administration. * 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 ...
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                          What is the average salary for Clinical Monitor in Ganshoren?

                          Average salary per year
                          42.200 €

                          The average salary for a Clinical Monitor in Ganshoren is 42.200 €. Clinical Monitor in Ganshoren salaries range from 35.200 € to 51.200 €.

                          Frequently Asked Questions

                          How many Clinical Monitor jobs are there in Ganshoren?
                          There are 14 Clinical Monitor jobs within 20 miles of Ganshoren available on StepStone right now.

                          What other similar jobs are there to Clinical Monitor jobs in Ganshoren?
                          As well as Clinical Monitor jobs in Ganshoren, you can find Sales, Communication, Projects, amongst many others.

                          Which skills are beneficial for Clinical Monitor jobs in Ganshoren?
                          The following skills are useful for Clinical Monitor jobs in Ganshoren: Communication, Projects, Business, Coordination, Budget.

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