Clinical Jobs in Antwerp Province

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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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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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(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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Secure Data Manager

SGS Group Belgium

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. 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. We have a challenge for a Secure Data Manager - Mechelen - 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,…). These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings. 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. 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. We have a challenge for a Secure Data Manager - Mechelen - 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,…). These responsibilities encompass the creation of data transfer agreements, data cleaning documentation and the specification of edit checks and listings.
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Programmer (Clinical Databases)

SGS Group Belgium

Mechelen

We are currently looking for Programmers (Mechelen)! As a Clinical Data Programmer, you are responsible for the set-up, structure and programming of the clinical data bases of the projects you are working on. 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. We are currently looking for Programmers (Mechelen)! As a Clinical Data Programmer, you are responsible for the set-up, structure and programming of the clinical data bases of the projects you are working on. 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.
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Medical Writer

SGS Group Belgium

Mechelen

We currently have an opportunity for a Medical Writer! 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. We currently have an opportunity for a Medical Writer! 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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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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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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Internship in Data Analysis

Robert Bosch NV/SA

Mechelen

You will be working as a Data Analytics Intern in the Sales and Operations department at Bosch Thermotechnology in Mechelen. You will maintain and harmonize the data present in different applications. You are currently a student (International Business Management, Marketing, Economical Studies, etc.) or you recently graduated, and you are interested in Data Analysis and Business Intelligence. If you are a student enrolled in a University/College outside of Belgium (or if you are available for a voluntary internship outside of your university curriculum) you will be granted an allowance of € 850/month. Robert Bosch NV/SA * Mechelen * Contract duration unspecified * Full Time - Smart and efficient – Bosch Thermotechnology offers its customers throughout the world solutions for their room climate, domestic hot water and decentralised energy management requirements. You will be working as a Data Analytics Intern in the Sales and Operations department at Bosch Thermotechnology in Mechelen. You will maintain and harmonize the data present in different applications. You are currently a student (International Business Management, Marketing, Economical Studies, etc.) or you recently graduated, and you are interested in Data Analysis and Business Intelligence. If you are a student enrolled in a University/College outside of Belgium (or if you are available for a voluntary internship outside of your university curriculum) you will be granted an allowance of € 850/month. Robert Bosch NV/SA * Mechelen * Contract duration unspecified * Full Time - Smart and efficient – Bosch Thermotechnology offers its customers throughout the world solutions for their room climate, domestic hot water and decentralised energy management requirements.
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Medical Affairs Associate

SGS Group Belgium

Mechelen

We are currently seeking for a Medical Affairs Associate. * Involved as internal and external contact for medical affairs projects - 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. This can only happen thanks to We are currently seeking for a Medical Affairs Associate. * Involved as internal and external contact for medical affairs projects - 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. This can only happen thanks to
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QA assistant

SGS Group Belgium

Mechelen

In the spirit of continued growth and to help improve our business, we are currently seeking for a QA assistant. As QA assistant in the preparation, audits in accordance with internal procedures. 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. In the spirit of continued growth and to help improve our business, we are currently seeking for a QA assistant. As QA assistant in the preparation, audits in accordance with internal procedures. 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.
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Regulatory Affairs Officer

Real Staffing Brussels (International)

Puurs

My clients Regulatory & Product Support Department is seeking a dynamic Regulatory Associate to join their team. You will work in cross-functional teams with different Puurs departments (manufacturing, labs, QA, supply,…) and collaborate with R&D, global regulatory colleagues (Global Chemistry, Manufacturing & Controls (GCMC)) and the supply department in order to support the introduction of new products in the site. * You support regulatory submissions (CTD, BLA) of the products by informing site colleagues of regulatory requirements and by authoring the dossier, for review with GCMC. In this regulatory role you interact on a daily basis with several Puurs departments (manufacturing, labs, QA, supply,…). * You assess Post approval changes at the manufacturing site and the associated regulatory variations. My clients Regulatory & Product Support Department is seeking a dynamic Regulatory Associate to join their team. You will work in cross-functional teams with different Puurs departments (manufacturing, labs, QA, supply,…) and collaborate with R&D, global regulatory colleagues (Global Chemistry, Manufacturing & Controls (GCMC)) and the supply department in order to support the introduction of new products in the site. * You support regulatory submissions (CTD, BLA) of the products by informing site colleagues of regulatory requirements and by authoring the dossier, for review with GCMC. In this regulatory role you interact on a daily basis with several Puurs departments (manufacturing, labs, QA, supply,…). * You assess Post approval changes at the manufacturing site and the associated regulatory variations.
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CMC Writer

Oxford Global Resources

Wavre

For one of our clients, located in Wavre, we our currently looking for 2 "CMC Writers". The Technical RA manager is responsible for the preparation, authoring and coordination of CMC submissions related to China Compliance remediations program. * Ensure coordination of activities related to CMC submission file preparation, including change control assessment, source documents collection from key contributing discipline (eg GIO,QC, Site Conformance, etc), initiation and management of CMC submission kick-off meeting,file authoring, review and approval. * Experience in CMC authoring of technical file - Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Job Description - The person will also be required to interact with regulatory and technical contributing disciplines Teams to ensure File content - definition, submission strategy and preparation coordination. For one of our clients, located in Wavre, we our currently looking for 2 "CMC Writers". The Technical RA manager is responsible for the preparation, authoring and coordination of CMC submissions related to China Compliance remediations program. * Ensure coordination of activities related to CMC submission file preparation, including change control assessment, source documents collection from key contributing discipline (eg GIO,QC, Site Conformance, etc), initiation and management of CMC submission kick-off meeting,file authoring, review and approval. * Experience in CMC authoring of technical file - Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Job Description - The person will also be required to interact with regulatory and technical contributing disciplines Teams to ensure File content - definition, submission strategy and preparation coordination.
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R&D Lab Leader

BIENCA NV

Gent

As R&D Lab Leader you are responsible for all activities related to QC and product development in the new lab. * Implement and maintain the lab quality system in the spirit of continuous improvement to comply with applicable standards (e.g. BRC) This interesting job requires you to have a sincere interest in applied R&D work for the food industry coupled with a good knowledge of microbiological test protocols in a lab environment. * Gent * Contract duration unspecified * Full Time - Based in the Ghent area, Bienca NV is a small-sized privately held Belgian company that develops and provides innovative and by nature inspired solutions for improving the microbial quality and safety of foods. The main product line, SEA-i®, is based on a natural enzymatic system and is used world-wide as an alternative to chemical preservatives. Your responsibilities - Function description - You . As R&D Lab Leader you are responsible for all activities related to QC and product development in the new lab. * Implement and maintain the lab quality system in the spirit of continuous improvement to comply with applicable standards (e.g. BRC) This interesting job requires you to have a sincere interest in applied R&D work for the food industry coupled with a good knowledge of microbiological test protocols in a lab environment. * Gent * Contract duration unspecified * Full Time - Based in the Ghent area, Bienca NV is a small-sized privately held Belgian company that develops and provides innovative and by nature inspired solutions for improving the microbial quality and safety of foods. The main product line, SEA-i®, is based on a natural enzymatic system and is used world-wide as an alternative to chemical preservatives. Your responsibilities - Function description - You .
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Data Manager

FERN VALLEY

East-Flanders

For the expansion of our client's clinical team, we are looking for a Clinical Data Manager (CDM). The CDM is responsible for all clinical data management aspects for the assigned global clinical studies from preparation until archiving. * Responsible for leading, guiding and overseeing the CROs data management activities and responsible for overseeing vendors involved in the assigned clinical studies based upon metrics and plan * contract negotiations together with the company's clinical study manager and Director Vendor Management * Providing input into and/or developing study related materials such as Clinical Study Protocol, Clinical Monitoring Plans, Data Management Plans, eCRF/EDC and Edit Check Specifications, eCRF completion guidelines, External Data Reconciliation Plans, SAS Listing Specifications, Lab Data Transfer Plans, etc. For the expansion of our client's clinical team, we are looking for a Clinical Data Manager (CDM). The CDM is responsible for all clinical data management aspects for the assigned global clinical studies from preparation until archiving. * Responsible for leading, guiding and overseeing the CROs data management activities and responsible for overseeing vendors involved in the assigned clinical studies based upon metrics and plan * contract negotiations together with the company's clinical study manager and Director Vendor Management * Providing input into and/or developing study related materials such as Clinical Study Protocol, Clinical Monitoring Plans, Data Management Plans, eCRF/EDC and Edit Check Specifications, eCRF completion guidelines, External Data Reconciliation Plans, SAS Listing Specifications, Lab Data Transfer Plans, etc.
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Innovation Manager in the field of Regenerative Medicine and Tissue Engineering

KU Leuven

Leuven

For Prometheus, the Division of Skeletal Tissue Engineering at KU Leuven, we are recruiting an Innovation Manager in Regenerative Medicine and Tissue Engineering. A team of more than 40 experienced Innovation Managers, embedded within research groups throughout the University and University Hospital, achieve this goal primarily by establishing mutually beneficial, collaborative relationships with a broad range of external partners in industry, academia, as well as national and regional public-private organizations. We offer a permanent position as Innovation Manager of the Industrial Research Fund (IOF) at KU Leuven, a world famous university. The goal of Industrial Research Fund (lOF) at KU Leuven, is to accelerate the transfer of knowledge and innovations arising from strategic basic research to the market. For Prometheus, the Division of Skeletal Tissue Engineering at KU Leuven, we are recruiting an Innovation Manager in Regenerative Medicine and Tissue Engineering. A team of more than 40 experienced Innovation Managers, embedded within research groups throughout the University and University Hospital, achieve this goal primarily by establishing mutually beneficial, collaborative relationships with a broad range of external partners in industry, academia, as well as national and regional public-private organizations. We offer a permanent position as Innovation Manager of the Industrial Research Fund (IOF) at KU Leuven, a world famous university. The goal of Industrial Research Fund (lOF) at KU Leuven, is to accelerate the transfer of knowledge and innovations arising from strategic basic research to the market.
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