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                          54 results for Clinical Monitor jobs in Mechelen within a 30 km radius

                          Medical Monitor (Gastroenterology)

                          Psi Cro Belgium BV
                          Leuven
                          Easy Apply
                          PSIMedical Monitorsprovide medical input to global clinical studies and advise the teams and business partners, 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
                          PSIMedical Monitorsprovide medical input to global clinical studies and advise the teams and business partners, 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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                          6-month internship - Group Process Transformation and Digitalisation

                          Eurofins Belgium
                          Brussels
                          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 continuously improvethe newly deployed process and associated tools.
                          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 continuously improvethe newly deployed process and associated tools.
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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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                          Contribute to global clinical trials involving digital pathology, whole slide imaging, and emerging technology platforms. * Analyze and respond to medical and pathology-related inquiries from clinical trial sponsors and investigators. * Participate in investigator meetings and client visits to provide pathology and medical support for clinical trials. * Additional subspecialty expertise or clinical pathology training
                          Contribute to global clinical trials involving digital pathology, whole slide imaging, and emerging technology platforms. * Analyze and respond to medical and pathology-related inquiries from clinical trial sponsors and investigators. * Participate in investigator meetings and client visits to provide pathology and medical support for clinical trials. * Additional subspecialty expertise or clinical pathology training
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                          Project Management: Actively participate in project management, monitor progress, coordinate actions with project teams and project managers, while respecting deadlines and budgets ;
                          Project Management: Actively participate in project management, monitor progress, coordinate actions with project teams and project managers, while respecting deadlines and budgets ;
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                          Our pharmaceutical-grade products are backed by rigorous clinical research, and our commitment to quality is at the heart of our success.
                          Our pharmaceutical-grade products are backed by rigorous clinical research, and our commitment to quality is at the heart of our success.
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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. The Clinical Research Laboratory Senior Technician's main responsibility includes proper sample management, storage and shipment on a day-to-day level. The Clinical Research Laboratory Senior Technician is responsible for the day-to-day Laboratory work. Ensure the control of the laboratory environment, safety specification, the maintenance and calibration of laboratory material required to conduct clinical trials. To attend to the Shift Report on the clinical floor in the morning and/or evening. Clinical skills - Successful study conduct of all Clinical Research Unit studies in accordance with ethical, legal, and moral standards, Good Clinical Practices (GCPs) and ISO 17025 requirements and drug development goals.
                          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. The Clinical Research Laboratory Senior Technician's main responsibility includes proper sample management, storage and shipment on a day-to-day level. The Clinical Research Laboratory Senior Technician is responsible for the day-to-day Laboratory work. Ensure the control of the laboratory environment, safety specification, the maintenance and calibration of laboratory material required to conduct clinical trials. To attend to the Shift Report on the clinical floor in the morning and/or evening. Clinical skills - Successful study conduct of all Clinical Research Unit studies in accordance with ethical, legal, and moral standards, Good Clinical Practices (GCPs) and ISO 17025 requirements and drug development goals.
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                          NEW
                          Monitors technical and regulatory developments and supports the progress of projects by analysing issues, conducting fact-finding activities, cross-checking sources, and proposing solutions or recommendations to relevant governing bodies.
                          Monitors technical and regulatory developments and supports the progress of projects by analysing issues, conducting fact-finding activities, cross-checking sources, and proposing solutions or recommendations to relevant governing bodies.
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                          Easy Apply
                          Support business development activities, including research and preparation of client materials * Monitor project progress, billing processes, and administrative follow-up
                          Support business development activities, including research and preparation of client materials * Monitor project progress, billing processes, and administrative follow-up
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                          A blend of creativity and analytical skills: you're able to both create compelling marketing content and to monitor and optimize it, figuring out what works and why.
                          A blend of creativity and analytical skills: you're able to both create compelling marketing content and to monitor and optimize it, figuring out what works and why.
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                          Easy Apply
                          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.
                          more
                          NEW
                          Develop and monitor operational KPIs to assess performance and adherence to client commitments. * Oversee budgets, monitor cash flow, and prepare financial forecasts.
                          Develop and monitor operational KPIs to assess performance and adherence to client commitments. * Oversee budgets, monitor cash flow, and prepare financial forecasts.
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                          NEW
                          Manage and monitor all installed systems and infrastructure * Monitor and test application performance for potential bottlenecks, identify possible solutions, and work with developers 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 developers to implement those fixes
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                          Easy Apply
                          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.
                          more

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                          What is the average salary for Clinical Monitor in Mechelen?

                          Average salary per year
                          45.100 €

                          The average salary for a Clinical Monitor in Mechelen is 45.100 €. Clinical Monitor in Mechelen salaries range from 36.900 € to 53.700 €.

                          Frequently Asked Questions

                          How many Clinical Monitor jobs are there in Mechelen?
                          There are 54 Clinical Monitor jobs within 20 miles of Mechelen available on StepStone right now.

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

                          Which skills are beneficial for Clinical Monitor jobs in Mechelen?
                          The following skills are useful for Clinical Monitor jobs in Mechelen: Communication, Business, Proactivity, Problem Management, Coordination.

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