Clinical jobs

In this role as QA Validation specialist you will define validation strategies in accordance with regulatory requirements and ensure compliance of validation activities at Eumedica site. As QA Validation Specialist, you . • Ensure QA oversight in validation activities (IQ/OQ/PQ...), through CCs, and ensure timely escalation to management of critical issues during validation • Participate in the implementation of the quality systems at Eumedica to ensure compliance and assurance for all validation activities on site like equipment, systems, IT, facilities, utilities • Define the validation strategies in accordance with the regulatory requirements for Eumedica projects and clinical customer projects • Define the validation strategies in accordance with the regulatory requirements • Review/Approve the validation documentation regarding the GMP requirements (knowledge of GMP, Eudralex, GAMP, CFR… In this role as QA Validation specialist you will define validation strategies in accordance with regulatory requirements and ensure compliance of validation activities at Eumedica site. As QA Validation Specialist, you . • Ensure QA oversight in validation activities (IQ/OQ/PQ...), through CCs, and ensure timely escalation to management of critical issues during validation • Participate in the implementation of the quality systems at Eumedica to ensure compliance and assurance for all validation activities on site like equipment, systems, IT, facilities, utilities • Define the validation strategies in accordance with the regulatory requirements for Eumedica projects and clinical customer projects • Define the validation strategies in accordance with the regulatory requirements • Review/Approve the validation documentation regarding the GMP requirements (knowledge of GMP, Eudralex, GAMP, CFR…
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PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health.
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Lead classrooms in the GE Academy together with subject matter experts and key opinion leaders * Become recognized expert in product/clinical technical competencies, answer a wide range of questions concerning software and clinical applications * Demonstrated skills in clinical scanning on current products / platforms * Clinical experience in hospital/university setting preferred - GE Healthcare * Diegem * Temporary * Full Time - About Us :GE (NYSE:GE) drives the world forward by tackling its biggest challenges. By combining world-class engineering with software and analytics, GE helps the world work more efficiently, reliably, and safely. GE people are global, diverse and dedicated, operating with the highest integrity and passion to fulfill GE's mission and deliver for our customers. The MRI ZCL will sites. Lead classrooms in the GE Academy together with subject matter experts and key opinion leaders * Become recognized expert in product/clinical technical competencies, answer a wide range of questions concerning software and clinical applications * Demonstrated skills in clinical scanning on current products / platforms * Clinical experience in hospital/university setting preferred - GE Healthcare * Diegem * Temporary * Full Time - About Us :GE (NYSE:GE) drives the world forward by tackling its biggest challenges. By combining world-class engineering with software and analytics, GE helps the world work more efficiently, reliably, and safely. GE people are global, diverse and dedicated, operating with the highest integrity and passion to fulfill GE's mission and deliver for our customers. The MRI ZCL will sites.
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The Senior Manager Microbiology Quality Control Quality Control Beerse. Janssen Pharmaceutica * Beerse * Contract duration unspecified * Full Time - Your tasks - Company Description 'Caring for the world, one person at a time'... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies in health care to touch the lives of over a billion people every day, throughout the world. Janssen Pharmaceutica joined the Johnson & Johnson group in 1961. Today, Janssen Pharmaceutica is one of the most innovative pharmaceutical companies in the world. The Senior Manager Microbiology Quality Control Quality Control Beerse. Janssen Pharmaceutica * Beerse * Contract duration unspecified * Full Time - Your tasks - Company Description 'Caring for the world, one person at a time'... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies in health care to touch the lives of over a billion people every day, throughout the world. Janssen Pharmaceutica joined the Johnson & Johnson group in 1961. Today, Janssen Pharmaceutica is one of the most innovative pharmaceutical companies in the world.
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Supports Project Management group with the development and implementation of study database design modifications. * Brussels * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. * Independently reviews clinical trial protocols and interprets Central Lab responsibilities based on protocol definitions and budgeted services. Supports Project Management group with the development and implementation of study database design modifications. * Brussels * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With offices in 47 countries and approximately 20,000 professionals worldwide, PPD applies innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development to deliver life-changing therapies that improve health. * Independently reviews clinical trial protocols and interprets Central Lab responsibilities based on protocol definitions and budgeted services.
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Acts as a main contact for Site ID tasks for the Site Intelligence and Selection Team in France and Benelux * Applies skills and discipline knowledge to Site Intelligence and Selection development projects * Manages Site IDs in France and Benelux by engaging with potential clinical sites and by reviewing internal and external intelligence on performance and quality metrics and performing literature research to to build the database. * Manages the generation and reporting of internal metrics for Study Optimization to support senior level discussions * Acts a system administrator of Pfizer’s Site Intelligence and Selection Tool to database and the collection of site intelligence data * Supports the Site Intelligence Lead to ensure knowledge of the goals, scope and requirements of the Site Feasibility project and ensure that high quality results are delivered. Acts as a main contact for Site ID tasks for the Site Intelligence and Selection Team in France and Benelux * Applies skills and discipline knowledge to Site Intelligence and Selection development projects * Manages Site IDs in France and Benelux by engaging with potential clinical sites and by reviewing internal and external intelligence on performance and quality metrics and performing literature research to to build the database. * Manages the generation and reporting of internal metrics for Study Optimization to support senior level discussions * Acts a system administrator of Pfizer’s Site Intelligence and Selection Tool to database and the collection of site intelligence data * Supports the Site Intelligence Lead to ensure knowledge of the goals, scope and requirements of the Site Feasibility project and ensure that high quality results are delivered.
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Overall objective: develop strategic path to reimbursement and execute on associated tactics to enable reimbursement for on-market products and new product development initiatives in assigned countries. Illumina UK * Belgium * Contract duration unspecified * Full Time - Do you want to make a difference? Illumina's mission is to improve human health by unlocking the power of the genome. If that inspires you, let's talk. We've built a culture fueled by innovation, collaboration and openness, and established ourselves as the global leader in DNA sequencing and array-based technologies. Our people and our technology change lives by driving advancements in life sciences, oncology, reproductive health, agriculture and other emerging markets. Life at Illumina is about working with teammates who are deeply passionate about what we do, because we know that our work has the power to improve lives. Overall objective: develop strategic path to reimbursement and execute on associated tactics to enable reimbursement for on-market products and new product development initiatives in assigned countries. Illumina UK * Belgium * Contract duration unspecified * Full Time - Do you want to make a difference? Illumina's mission is to improve human health by unlocking the power of the genome. If that inspires you, let's talk. We've built a culture fueled by innovation, collaboration and openness, and established ourselves as the global leader in DNA sequencing and array-based technologies. Our people and our technology change lives by driving advancements in life sciences, oncology, reproductive health, agriculture and other emerging markets. Life at Illumina is about working with teammates who are deeply passionate about what we do, because we know that our work has the power to improve lives.
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We are currently looking for Programmers ! 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 - Introduction - Introductie - 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 Programmers ! 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 - Introduction - Introductie - 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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As a Sales Representative, you are responsible for pro-active sales of BDI PI products. As a Sales Representative you report to the Sales & Key Account Director BD Interventional Benelux. To strengthen the team of BDI Interventional Benelux, we are looking for a Sales Representative Peripheral Intervention. * You have experience within and understanding of the hospital environment as well as the ability to demonstrate a successful track record in selling to both senior clinical and commercial business managers in a hospital setting - While positively representing the company, meeting and exceeding sales targets, increasing the market share and market presence in the respective assigned region. * You execute all sales activity from new product introduction such as instruction and presentation to customers, to handling contract negotiations and monitoring the deal until closure. As a Sales Representative, you are responsible for pro-active sales of BDI PI products. As a Sales Representative you report to the Sales & Key Account Director BD Interventional Benelux. To strengthen the team of BDI Interventional Benelux, we are looking for a Sales Representative Peripheral Intervention. * You have experience within and understanding of the hospital environment as well as the ability to demonstrate a successful track record in selling to both senior clinical and commercial business managers in a hospital setting - While positively representing the company, meeting and exceeding sales targets, increasing the market share and market presence in the respective assigned region. * You execute all sales activity from new product introduction such as instruction and presentation to customers, to handling contract negotiations and monitoring the deal until closure.
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Your role as HR Business Partner will be to “life cycle” processes from onboarding to development. Your main mission will be to develop HR activities to attract and retain talents. * You own a Master Degree ideally in HR, Psychology, Social Law or Economics - PlusOne * Walloon Brabant * Contract duration unspecified * Part time - Introduction - Medical Devices – Part-Time - Therefore your responsibilities will be divided in 2 main activities: Talent Acquisition and Staff Management. Your tasks - Talent Acquisition * Prepare and review the annual recruitment Plan with the Steering Committee. * Lead the attraction and selection process in collaboration with key stakeholders within the organization. * Equip and with the right skills and tools to select the best talent. * Manage, update and maintain the various recruitment communication channels (websites, social media). Your role as HR Business Partner will be to “life cycle” processes from onboarding to development. Your main mission will be to develop HR activities to attract and retain talents. * You own a Master Degree ideally in HR, Psychology, Social Law or Economics - PlusOne * Walloon Brabant * Contract duration unspecified * Part time - Introduction - Medical Devices – Part-Time - Therefore your responsibilities will be divided in 2 main activities: Talent Acquisition and Staff Management. Your tasks - Talent Acquisition * Prepare and review the annual recruitment Plan with the Steering Committee. * Lead the attraction and selection process in collaboration with key stakeholders within the organization. * Equip and with the right skills and tools to select the best talent. * Manage, update and maintain the various recruitment communication channels (websites, social media).
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After a strong experience as CRA, you want to endorse new responsibilities as Clinical Study Manager? • You ensure that assigned clinical study project(s) are managed in respect of established timelines and quality and regulatory standards. • You develop and manage study-related documents and necessary structures for efficient running of clinical studies. Thanks to that operational experience of Clinical activities you want to bring your expertise to a more helicopter level? specialized in improving clinical outcome of patients with impaired cardiac function, active in interventional cardiology. The technology is in advanced clinical stage, with various potential therapeutic applications. This unique and interesting role is to serve as a path to clinical project management duties for a well-established CRA willing advance in their career. After a strong experience as CRA, you want to endorse new responsibilities as Clinical Study Manager? • You ensure that assigned clinical study project(s) are managed in respect of established timelines and quality and regulatory standards. • You develop and manage study-related documents and necessary structures for efficient running of clinical studies. Thanks to that operational experience of Clinical activities you want to bring your expertise to a more helicopter level? specialized in improving clinical outcome of patients with impaired cardiac function, active in interventional cardiology. The technology is in advanced clinical stage, with various potential therapeutic applications. This unique and interesting role is to serve as a path to clinical project management duties for a well-established CRA willing advance in their career.
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The Regulatory Affairs Registration Manager is responsible for the maintenance of the worldwide vaccine licences. by ensuring the planning/dispatch/submission/follow-up/approval of data-packages due to Regulatory Authorities: Variations, Commitments, Questions & Answers, PSURs/PBRERs, Risk Management Plans (RMPs), Renewals, Articles 46, Updated files, WHO Annual Reports, New Dossier requests etc … (labelling/safety/epidemiology/clinical and technical Experts) for the preparation of the documents part of the regulatory dossiers/data-packages in order to meet the submission timelines - Ensure that all regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations to Authorities are closely monitored and fullfilled - Exhibit a very good understanding and ensure alignment with regulatory legislation/guidelines, particularly relating to administrative and procedural aspects The Regulatory Affairs Registration Manager is responsible for the maintenance of the worldwide vaccine licences. by ensuring the planning/dispatch/submission/follow-up/approval of data-packages due to Regulatory Authorities: Variations, Commitments, Questions & Answers, PSURs/PBRERs, Risk Management Plans (RMPs), Renewals, Articles 46, Updated files, WHO Annual Reports, New Dossier requests etc … (labelling/safety/epidemiology/clinical and technical Experts) for the preparation of the documents part of the regulatory dossiers/data-packages in order to meet the submission timelines - Ensure that all regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations to Authorities are closely monitored and fullfilled - Exhibit a very good understanding and ensure alignment with regulatory legislation/guidelines, particularly relating to administrative and procedural aspects
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For one of our clients located in the east of Brussels, we are looking for an enthusiastic Clinical Data Manager (M/F). As Clinical Data Manager, you . You are responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection, review and validation of the clinical data in a timely manner; this to ensure adequacy, integrity and quality of the data that are used to answer the questions of the studies. * Development of the Data Management sections of the clinical trial protocol Clinical trial protocol * Assisting in the final review of the clinical trial protocol for consistence Data handling * Coordination and control of data collection, data cleaning and data reporting activities * Application of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements. For one of our clients located in the east of Brussels, we are looking for an enthusiastic Clinical Data Manager (M/F). As Clinical Data Manager, you . You are responsible for all the steps required for the setup of the Data Management tools of a clinical trial and for the collection, review and validation of the clinical data in a timely manner; this to ensure adequacy, integrity and quality of the data that are used to answer the questions of the studies. * Development of the Data Management sections of the clinical trial protocol Clinical trial protocol * Assisting in the final review of the clinical trial protocol for consistence Data handling * Coordination and control of data collection, data cleaning and data reporting activities * Application of QC to each stage in the data handling to ensure the data are reliable and processed in compliance with ICH-GCP requirements.
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Our writing team is looking for Medical Writers . Modis LS offers a unique combination of providing high qualified Scientific, Technical, Commercial and/or Medical expertise through staffing, consultancy, Project management or Project delivery services. We have more than 350 talents helping out our clients in different phases of the development process of a drug/medical device or product. Medical writing skills (write/edit content, format style, grammar, logic and consistency, present complex datasets in a clear and visual way) Modis Belgium * Wavre * Contract duration unspecified * Full Time - Are you ready for a new experience? Come and be part of Modis Life Sciences (part of Adecco Grouop, Great Place to work!) You'll will be part of an international team full of passion! Your tasks Our writing team is looking for Medical Writers . Modis LS offers a unique combination of providing high qualified Scientific, Technical, Commercial and/or Medical expertise through staffing, consultancy, Project management or Project delivery services. We have more than 350 talents helping out our clients in different phases of the development process of a drug/medical device or product. Medical writing skills (write/edit content, format style, grammar, logic and consistency, present complex datasets in a clear and visual way) Modis Belgium * Wavre * Contract duration unspecified * Full Time - Are you ready for a new experience? Come and be part of Modis Life Sciences (part of Adecco Grouop, Great Place to work!) You'll will be part of an international team full of passion! Your tasks
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At Modis, we are hiring a Clinical LaboratoryScientific writer to join our international team. Modis Belgium * Wavre * Contract duration unspecified * Full Time - You'll write scientific and technical documents to support clinical laboratories activities, as well as write and edit various clinical documents and publications as per international guidelines and company policies and procedures. Your tasks - o Procedures - o Technical protocols & reports (e.g. clinical assay validation) o Answers to questions from Authorities - o Briefing documents - o Translations - High quality writing (clear, concise, plain, correct grammar and spelling, correct formatting) Excellent management of development of documents from first draft to finalize document (planning, interaction/ , resolution of comments, facilitation) Respect of timelines - Ensure compliance with applicable procedures and requirements At Modis, we are hiring a Clinical LaboratoryScientific writer to join our international team. Modis Belgium * Wavre * Contract duration unspecified * Full Time - You'll write scientific and technical documents to support clinical laboratories activities, as well as write and edit various clinical documents and publications as per international guidelines and company policies and procedures. Your tasks - o Procedures - o Technical protocols & reports (e.g. clinical assay validation) o Answers to questions from Authorities - o Briefing documents - o Translations - High quality writing (clear, concise, plain, correct grammar and spelling, correct formatting) Excellent management of development of documents from first draft to finalize document (planning, interaction/ , resolution of comments, facilitation) Respect of timelines - Ensure compliance with applicable procedures and requirements
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You are supported by the R&D Project Planner and you . * Report project progress and delivery to program manager. You take ownership of various projects, from initiation to planning, execution, monitoring, controlling and delivery. You coordinate functional project teams within a specific domain of the drug development cycle. By putting your talents and ambitions first, we can offer you projects that inspire, challenge and reward you – all in line with your unique profile. Thanks to our broad network, we can connect you with diverse internal and external careers and projects in Life Sciences. * Translate scientific strategy into project plan and create project charter, taking in account cross-functional interdependencies. * Own project budget, monitor and optimize project planning, control resources. You are supported by the R&D Project Planner and you . * Report project progress and delivery to program manager. You take ownership of various projects, from initiation to planning, execution, monitoring, controlling and delivery. You coordinate functional project teams within a specific domain of the drug development cycle. By putting your talents and ambitions first, we can offer you projects that inspire, challenge and reward you – all in line with your unique profile. Thanks to our broad network, we can connect you with diverse internal and external careers and projects in Life Sciences. * Translate scientific strategy into project plan and create project charter, taking in account cross-functional interdependencies. * Own project budget, monitor and optimize project planning, control resources.
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The Program Coordinator (PML) and Clinical Program Management Leader (CPML) in providing and maintaining cross functional project plans utilizing systems and tools aligned across R&D. We are looking for a Program Coordinator * Assists the Program Management Leader (PML) in providing and maintaining system tools and cross-functional project plans aligned across R&D (Clinical, Pre-Clinical, CDOs, CPS, Biomarker, and PDMS) to . Modis Belgium * Temse * Contract duration unspecified * Full Time - At Modis, we prioritize your professional development. By putting your talents and ambitions first, we can offer you projects that inspire, challenge and reward you – all in line with your unique profile. Find the perfect fit Your working environment matters to us. Thanks to our broad network, we can connect you with diverse internal and external careers and projects in life sciences, IT and engineering. The Program Coordinator (PML) and Clinical Program Management Leader (CPML) in providing and maintaining cross functional project plans utilizing systems and tools aligned across R&D. We are looking for a Program Coordinator * Assists the Program Management Leader (PML) in providing and maintaining system tools and cross-functional project plans aligned across R&D (Clinical, Pre-Clinical, CDOs, CPS, Biomarker, and PDMS) to . Modis Belgium * Temse * Contract duration unspecified * Full Time - At Modis, we prioritize your professional development. By putting your talents and ambitions first, we can offer you projects that inspire, challenge and reward you – all in line with your unique profile. Find the perfect fit Your working environment matters to us. Thanks to our broad network, we can connect you with diverse internal and external careers and projects in life sciences, IT and engineering.
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Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. * PhD degree in statistics or biostatistics or Master's degree with relevant experience required. Bristol-Myers Squibb Co. * Braine l'Alleud * Contract duration unspecified * Full Time - One shared journey moves us forward. Bristol-Myers Squibb is a BioPharma leader offering opportunities to learn and grow professionally, working alongside smart, talented colleagues who are committed to helping patients prevail over serious diseases. Our medicines help millions of people around the world in their fight against cancer, heart disease, HCV, and rheumatoid arthritis. Takes accountability for ensuring quality in all planning, design and execution of assignments associated with the assigned protocol or project. * PhD degree in statistics or biostatistics or Master's degree with relevant experience required. Bristol-Myers Squibb Co. * Braine l'Alleud * Contract duration unspecified * Full Time - One shared journey moves us forward. Bristol-Myers Squibb is a BioPharma leader offering opportunities to learn and grow professionally, working alongside smart, talented colleagues who are committed to helping patients prevail over serious diseases. Our medicines help millions of people around the world in their fight against cancer, heart disease, HCV, and rheumatoid arthritis.
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