SGS Group Belgium jobs in Mechelen

We have a challenge for a SAS Programmer / Master Statistics - Mechelen - You create, program and validate SAS datasets and you get the possibility to create randomisation lists. On the technical side you have knowledge of SAS (BASE-STAT-macros-…) in order to solve SAS programming errors, create SAS datasets, create and validate new SAS macros, create and document specifications / requirements of SAS datasets,… 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. We have a challenge for a SAS Programmer / Master Statistics - Mechelen - You create, program and validate SAS datasets and you get the possibility to create randomisation lists. On the technical side you have knowledge of SAS (BASE-STAT-macros-…) in order to solve SAS programming errors, create SAS datasets, create and validate new SAS macros, create and document specifications / requirements of SAS datasets,… 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.
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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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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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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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We are currently looking for Clinical Data Managers - Masters in Biomedical Sciences (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; You have obtained a Master's Degree in a paramedical area or biomedical sciences. 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; SGS Group Belgium * Mechelen * Not available * Full Time - Company Description - At SGS, you can choose! We are currently looking for Clinical Data Managers - Masters in Biomedical Sciences (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; You have obtained a Master's Degree in a paramedical area or biomedical sciences. 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; SGS Group Belgium * Mechelen * Not available * Full Time - Company Description - At SGS, you can choose!
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We are currently looking for an EDC Assistant. The responsibility of the EDC Assistant is to assist the EDC (Electronic Data Capture) department with project related and/or general administrative work. * You have obtained a bachelor's degree in Office Management or you are a Management Assistant (medical secretary is a plus) or equivalent through experience; SGS Group Belgium * Mechelen * Not available * 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. We are currently looking for an EDC Assistant. The responsibility of the EDC Assistant is to assist the EDC (Electronic Data Capture) department with project related and/or general administrative work. * You have obtained a bachelor's degree in Office Management or you are a Management Assistant (medical secretary is a plus) or equivalent through experience; SGS Group Belgium * Mechelen * Not available * 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.
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We currently have an opportunity for a Medical Writer! SGS Group Belgium * Mechelen * Not available * 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. We currently have an opportunity for a Medical Writer! SGS Group Belgium * Mechelen * Not available * 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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In the spirit of continued growth and to help improve our business, we are currently looking for a Biostatistical Analyst SGS Group Belgium * Mechelen * Not available * 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 looking for a Biostatistical Analyst SGS Group Belgium * Mechelen * Not available * 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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As a Lead Cloud Developer (Azure) you get to play a key role in the analysis, architecture, design, development, implementation, integration and support of maintainable, scalable and robust cloud solutions always with cost containment strategies in mind. We are currently looking for a (m/f): Lead Cloud Developer (Azure) - Mechelen - You have a strong preference for a cloud-native approach and can also modernize existing applications - You provide consultation, guidance, and support across existing and emerging cloud technologies to the team - Using the Agile methodology you design, build and maintain efficient, reusable and reliable cloud solutions. You have proven work experience in a .NET and Azure development environment in order to get data management applications to the cloud A team player you can , end-users, Project Leads, testers and the validation team - SGS Group Belgium * Mechelen * Not available As a Lead Cloud Developer (Azure) you get to play a key role in the analysis, architecture, design, development, implementation, integration and support of maintainable, scalable and robust cloud solutions always with cost containment strategies in mind. We are currently looking for a (m/f): Lead Cloud Developer (Azure) - Mechelen - You have a strong preference for a cloud-native approach and can also modernize existing applications - You provide consultation, guidance, and support across existing and emerging cloud technologies to the team - Using the Agile methodology you design, build and maintain efficient, reusable and reliable cloud solutions. You have proven work experience in a .NET and Azure development environment in order to get data management applications to the cloud A team player you can , end-users, Project Leads, testers and the validation team - SGS Group Belgium * Mechelen * Not available
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We are currently looking for an e-CRF Designer – Master in Sciences (Mechelen) The main tasks of the (e-)CRF Designer ((e-)CRF-D) consist of designing data collection tools (DCT) (e-CRFs or paper CRFs) based on a clinical trial protocol and the sponsor's requirements and specifications. SGS Group Belgium * Mechelen * Not available * 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. We are currently looking for an e-CRF Designer – Master in Sciences (Mechelen) The main tasks of the (e-)CRF Designer ((e-)CRF-D) consist of designing data collection tools (DCT) (e-CRFs or paper CRFs) based on a clinical trial protocol and the sponsor's requirements and specifications. SGS Group Belgium * Mechelen * Not available * 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.
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In the role of Director QA, You are part of the Clinical to the operational teams and the Managing Director. Your responsibilities as our Director QA?! Our Director of Quality Assurance (DQA) gets the opportunity to develop, establish and oversee our QA systems and processes to ensure high quality client services, clinical research processes and compliance with regulatory requirements. o Responsibility, confidentiality, integrity are crucial to become a successful QA Director On top of that you have the ability to communicate a clear strategic vision for QA and the ability to anticipate and prevent quality and/or regulatory problems. * Managing the QA department, which consists of 10+ people! * You set clear objectives for performance and accountability for the QA team In the role of Director QA, You are part of the Clinical to the operational teams and the Managing Director. Your responsibilities as our Director QA?! Our Director of Quality Assurance (DQA) gets the opportunity to develop, establish and oversee our QA systems and processes to ensure high quality client services, clinical research processes and compliance with regulatory requirements. o Responsibility, confidentiality, integrity are crucial to become a successful QA Director On top of that you have the ability to communicate a clear strategic vision for QA and the ability to anticipate and prevent quality and/or regulatory problems. * Managing the QA department, which consists of 10+ people! * You set clear objectives for performance and accountability for the QA team
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We are currently looking for a Clinical Trial Assistant (Mechelen). 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. * Preparing, updating, follow-up of electronic filing of clinical trial related documents * Entering, updating and tracking of records in the Clinical Trial Management System * You have a bachelor degree 'Medical/Administrative assistant' or equivalent by relevant experience * Clinical experience as well as eTMF experience is a plus! 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 currently looking for a Clinical Trial Assistant (Mechelen). 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. * Preparing, updating, follow-up of electronic filing of clinical trial related documents * Entering, updating and tracking of records in the Clinical Trial Management System * You have a bachelor degree 'Medical/Administrative assistant' or equivalent by relevant experience * Clinical experience as well as eTMF experience is a plus! 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?
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We are currently looking for Clinical Database Programmers (Mechelen)! As a Clinical Data Programmer, you are working project related (your project = a clinical study) in a clinical study team within Data Management. 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. You are responsible for the setup of the SDTM (Study Data Tabulation Model) or clinical back-end database which will serve as the Meta Data Repository for your study. - You program the cleaning rules (SQL) described by the Clinical Data Manager on your studies and are responsible for the Metadata of your trial We are currently looking for Clinical Database Programmers (Mechelen)! As a Clinical Data Programmer, you are working project related (your project = a clinical study) in a clinical study team within Data Management. 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. You are responsible for the setup of the SDTM (Study Data Tabulation Model) or clinical back-end database which will serve as the Meta Data Repository for your study. - You program the cleaning rules (SQL) described by the Clinical Data Manager on your studies and are responsible for the Metadata of your trial
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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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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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