Jobs en tant que Technical Jobs à Mechelen

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EDC Validation Expert

SGS Group Belgium

Mechelen

The EDC Validation Expert makes the eCRF, IXRS and/or ePRO-tools fit for use and tests tool specifications through User Acceptance Testing, based on the clinical trial protocol and sponsor's requirements. * You would never like to stop learning, you have a great hunger for knowledge and are persistent to become the best EDC Validation Expert out there. Next to all the digital tasks, you will also provide expert guidance to the design and validation of EDC applications and you always and system providers throughout the whole process * Generate and maintain functional specifications for the EDC tool Data Validation Rules * Create test steps and validation documents for User Acceptance Testing of eCRF, IXRS and ePRO tools - SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. The EDC Validation Expert makes the eCRF, IXRS and/or ePRO-tools fit for use and tests tool specifications through User Acceptance Testing, based on the clinical trial protocol and sponsor's requirements. * You would never like to stop learning, you have a great hunger for knowledge and are persistent to become the best EDC Validation Expert out there. Next to all the digital tasks, you will also provide expert guidance to the design and validation of EDC applications and you always and system providers throughout the whole process * Generate and maintain functional specifications for the EDC tool Data Validation Rules * Create test steps and validation documents for User Acceptance Testing of eCRF, IXRS and ePRO tools - SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies.
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Head Clinical Project Management

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a Head Clinical Project Management. As Head Clinical Project Management (HCPM) (CPM) and ensure the allocation of the appropriate CPM resource to the projects. As HCPM, you may assume the responsibilities of a Project Manager in the management of clinical research projects. * Line management: managing and coaching the clinical project management team, providing them with support, advice and assistance, evaluating their training needs, organizing regular team meetings in order to control the execution of different projects (budget, planning, resources, quality, problems, …), performing annual appraisals and defining the performance objectives, … * Resource management: CO in the recruitment of new CPMs, evaluating the CPM workload, assigning a CPM to new projects, … In the spirit of continued growth and to help improve our business, we are currently seeking for a Head Clinical Project Management. As Head Clinical Project Management (HCPM) (CPM) and ensure the allocation of the appropriate CPM resource to the projects. As HCPM, you may assume the responsibilities of a Project Manager in the management of clinical research projects. * Line management: managing and coaching the clinical project management team, providing them with support, advice and assistance, evaluating their training needs, organizing regular team meetings in order to control the execution of different projects (budget, planning, resources, quality, problems, …), performing annual appraisals and defining the performance objectives, … * Resource management: CO in the recruitment of new CPMs, evaluating the CPM workload, assigning a CPM to new projects, …
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Contract Coördinator

SGS Group Belgium

Mechelen

SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose! First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose! First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. Our coworkers build their own way inside the company, the services and the expertise.
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Project Manager Biometrics

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a Project Manager Biometrics As Project Manager Biometrics you will manage a cross-functional team in the execution of the biometric and medical affairs (medical review and pharmacovigilance) aspects of a clinical trial. You will be the biometrics primary contact to the sponsor, the other SGS Life Science project related team and the external biometrics providers. Your main responsibility is to plan, organize, coordinate and control the project-related biometric activities in order to achieve all the objectives described in the contract within the constraints of timelines and budget and with respect to ICH-GCP and the applicable procedures. * You follow up on the status of the project * You will be the primary contact person in case of project audits. In the spirit of continued growth and to help improve our business, we are currently seeking for a Project Manager Biometrics As Project Manager Biometrics you will manage a cross-functional team in the execution of the biometric and medical affairs (medical review and pharmacovigilance) aspects of a clinical trial. You will be the biometrics primary contact to the sponsor, the other SGS Life Science project related team and the external biometrics providers. Your main responsibility is to plan, organize, coordinate and control the project-related biometric activities in order to achieve all the objectives described in the contract within the constraints of timelines and budget and with respect to ICH-GCP and the applicable procedures. * You follow up on the status of the project * You will be the primary contact person in case of project audits.
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Master in Sciences - Clinical Data Manager

SGS Group Belgium

Mechelen

We are currently looking for Clinical Data Managers (Mechelen). You will be in charge of data cleaning of clinical subject databases. You check clinical databases on inconsistent, missing and incorrect data and make sure mistakes are found either way; SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. will define the cleaning package of a clinical trial; You will generate queries towards the sites to get the data clean and will not give up until you reach your goal; you love to communicate with all involved parties. You have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time We are currently looking for Clinical Data Managers (Mechelen). You will be in charge of data cleaning of clinical subject databases. You check clinical databases on inconsistent, missing and incorrect data and make sure mistakes are found either way; SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. will define the cleaning package of a clinical trial; You will generate queries towards the sites to get the data clean and will not give up until you reach your goal; you love to communicate with all involved parties. You have obtained a Master's Degree in a paramedical area or biomedical sciences. SGS Group Belgium * Mechelen * Contract duration unspecified * Full Time
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Clincal Research Coordinator

SGS Group Belgium

Antwerpen

In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Research Coordinator. SGS Group Belgium * Antwerpen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures. In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Research Coordinator. SGS Group Belgium * Antwerpen * Contract duration unspecified * Full Time - Company Description - At SGS, you can choose. First of all, out of our various vacancies. However, SGS also gives you another choice. Do you choose to expand or to enrich? We are not only looking for colleagues who can go in to depths of their discipline. We are equally as much looking for colleagues who we call 'connectors', people who can connect our diversity to our services. To each other. And this way, enrich our business. SGS is the world's leading inspection, verification, testing and certification company. We're also the benchmark worldwide for quality and integrity. And that makes us very proud. Our employees give 110% of themselves every day, divided over all expertises, branches and cultures.
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Clinical Project Manager (Phase II-III)

SGS Group Belgium

Mechelen

As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. As Clinical Project Manager (CPM) at SGS you will provide leadership to a (cross-functional) team in the execution of clinical research projects (late phases). In the spirit of continued growth and to help improve our business, we are currently seeking for a Clinical Project Manager (Phase II-III). * You have at least 2 years of experience in an International Project Management role, having managed international phase 2 and 3 clinical trials in a pharmaceutical or biotech company or another CRO. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities.
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Business Development Manager Clinical research (Benelux)

SGS Group Belgium

Mechelen

As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business in order to maximize organization growth. In the spirit of continued growth and to help improve our business, we are currently seeking for a Business Development Manager Clinical Research (Northern Europe). * that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business; * You have experience within the fields of Clinical research and CRO business, or other associated, relevant businesses. * that you will further develop and maintain business development databases. As Business Development Manager you will be responsible for identifying and exploring strategic business development opportunities within the Clinical Research business in order to maximize organization growth. In the spirit of continued growth and to help improve our business, we are currently seeking for a Business Development Manager Clinical Research (Northern Europe). * that with your extensive knowledge of current market evolutions and conditions you will be responsible for the growth of our Clinical research Business with both new and existing customers, with an emphasis on customer satisfaction and repeat business; * You have experience within the fields of Clinical research and CRO business, or other associated, relevant businesses. * that you will further develop and maintain business development databases.
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(Senior) Clinical Data Manager (CDM)

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a (Senior) Clinical Data Manager (CDM). * Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … As an experienced CDM you are the Data Management the (Data Management) (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities. In the spirit of continued growth and to help improve our business, we are currently seeking for a (Senior) Clinical Data Manager (CDM). * Communication with all involved parties (EDC, STAT, MA, Clinical teams, Client, External Data Providers, Medical Writing, Project Manager Biometrics) … As an experienced CDM you are the Data Management the (Data Management) (DM) Lead who is, overall responsible for all the DM activities from the projects on which you are assigned. * Preferably, a minimum of 2 years of experience within Clinical Trial Data Management is required. SGS Life Sciences carries out all type of services for pharmaceutical and biotechnology companies, from coordination and running of clinical trials with new molecules or techniques on human beings, to support and consultancy on post marketing registration activities.
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QA manager

Brunel Belgium NV

Vlaams-Brabant

At the moment for example, we are looking for a quality assurance manager to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Follow-up of Quality-KPI's. * Review and alignment of Quality Technical Agreements with customers as well as with suppliers. At the moment for example, we are looking for a quality assurance manager to consult one of out clients. * Minimum 5 years of experience in a QA-position, preferably in the Pharmaceutical-related Industry - Brunel Belgium NV * Vlaams-Brabant * Contract duration unspecified * Full Time - About You - As a consultancy company specialized in Life Sciences, Infrastructure and IT we are looking for new consultants to . Your responsibilities * Advising on the translation of GDP-, GMP- and customer requirements that need to be integrated in the operational processes. Ensure the incorporation of such requirements in the procedures and instructions and provide training when necessary. * Follow-up of Quality-KPI's. * Review and alignment of Quality Technical Agreements with customers as well as with suppliers.
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R&D Manager

Umicore

Olen

You will be responsible for managing R&D projects and supervising a direct report. Umicore * Olen * Contract duration unspecified * Full Time - About Umicore - Reducing harmful vehicle emissions. Giving new life to used metals. Powering the cars of the future. As a global materials and technology group, we pioneer approaches to sustainability that continue to offer customers materials and solutions that are essential to everyday life. We aim to be a clear world leader in materials for clean mobility and recycling and have turned our sustainability approach into an even greater competitive advantage. To achieve this, however, we know we can't stand still. We know we need to find new ways to do things, discover new solutions and develop new ideas. It's why we invest so much in research & development. It's why we push ourselves to tackle increasingly complex challenges. You will be responsible for managing R&D projects and supervising a direct report. Umicore * Olen * Contract duration unspecified * Full Time - About Umicore - Reducing harmful vehicle emissions. Giving new life to used metals. Powering the cars of the future. As a global materials and technology group, we pioneer approaches to sustainability that continue to offer customers materials and solutions that are essential to everyday life. We aim to be a clear world leader in materials for clean mobility and recycling and have turned our sustainability approach into an even greater competitive advantage. To achieve this, however, we know we can't stand still. We know we need to find new ways to do things, discover new solutions and develop new ideas. It's why we invest so much in research & development. It's why we push ourselves to tackle increasingly complex challenges.
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Data Expert - Master or PhD (Biomedical) Sciences

SGS Group Belgium

Mechelen

We have a challenge for a Secure Data Manager - Mechelen - The Secure Data Manager will be responsible for the transfer of unblinding data from and to the Secure Data Office and the cleaning of unblinding data within the Secure Data Office. These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings. The Secure Data Manager also performs the QC of unblinding data, the cleaning of the data in EDC and/or clinical database and the creation/follow-up of edit checks. In addition to the above mentioned activities, the Secure Data Manager will also be responsible for the handling of randomisation lists (upload of randomisation list in internal IWRS system, release of randomisation list at database lock, emergency unblindings, distribution of randomisation list to third parties,…). We have a challenge for a Secure Data Manager - Mechelen - The Secure Data Manager will be responsible for the transfer of unblinding data from and to the Secure Data Office and the cleaning of unblinding data within the Secure Data Office. These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings. The Secure Data Manager also performs the QC of unblinding data, the cleaning of the data in EDC and/or clinical database and the creation/follow-up of edit checks. In addition to the above mentioned activities, the Secure Data Manager will also be responsible for the handling of randomisation lists (upload of randomisation list in internal IWRS system, release of randomisation list at database lock, emergency unblindings, distribution of randomisation list to third parties,…).
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