Clinical jobs

A strong scientific merit is required - must be perceived as a peer by the customer base (MD, PharmD., Pharmacist, PhD, advanced degree in medical or other life sciences) Do you have a solid scientific background (knowledge of cardiology is a big asset) and looking forward to an opportunity in Medical Affairs? * Medical Experts (ME) Development and Management: Identify, develop, and collaborate with current and future thought leaders. * Medical Education and Communication: Educate ME, speakers, investigators and other external customers (e.g Hospital and other Health Committees) on novel and emerging data as per Scientific Operations and local business unit objectives/priorities. Foster medical and scientific information exchange between the medical community and the company. A strong scientific merit is required - must be perceived as a peer by the customer base (MD, PharmD., Pharmacist, PhD, advanced degree in medical or other life sciences) Do you have a solid scientific background (knowledge of cardiology is a big asset) and looking forward to an opportunity in Medical Affairs? * Medical Experts (ME) Development and Management: Identify, develop, and collaborate with current and future thought leaders. * Medical Education and Communication: Educate ME, speakers, investigators and other external customers (e.g Hospital and other Health Committees) on novel and emerging data as per Scientific Operations and local business unit objectives/priorities. Foster medical and scientific information exchange between the medical community and the company.
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Are you a Senior Health Economists with experience in evidence generation and confidence with programming in EXCEL, VBA, R and/or Matlab ? * Development of publication/poster potentially but not necessarily in collaboration with Key External Experts; Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Would you like to work for a well-known pharmaceutical company located in Waver? Also fluent in English? Then we probably have THE job for you ! Job description - The mission of the Health Economics Support in the Vaccines Value Evidence team is a global role for specific tasks as well as potentially leading the implementation of targeted projects. In line with the CW Clinical_Health Economics Support role description, the mission for this contingent worker (CW) would include evidence generation and modelling activities. Are you a Senior Health Economists with experience in evidence generation and confidence with programming in EXCEL, VBA, R and/or Matlab ? * Development of publication/poster potentially but not necessarily in collaboration with Key External Experts; Oxford Global Resources * Wavre * Contract duration specified * Full Time - Your responsibilities - Would you like to work for a well-known pharmaceutical company located in Waver? Also fluent in English? Then we probably have THE job for you ! Job description - The mission of the Health Economics Support in the Vaccines Value Evidence team is a global role for specific tasks as well as potentially leading the implementation of targeted projects. In line with the CW Clinical_Health Economics Support role description, the mission for this contingent worker (CW) would include evidence generation and modelling activities.
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We currently have an opportunity for a CRA to join our Clinical Monitoring department in Belgium as a CRA II or Senior CRA, depending on experience. * Minimum 1+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation - Our global Clinical Monitoring department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. Together, we help clients define and develop clinical programmes, minimise delays and execute high-quality, cost-efficient clinical studies. * Perform and coordinate all aspects of the clinical monitoring process. * Nationwide * Contract duration unspecified * Full Time - We are vital links between an idea for a new medicine and the people who need it. We currently have an opportunity for a CRA to join our Clinical Monitoring department in Belgium as a CRA II or Senior CRA, depending on experience. * Minimum 1+ year of Independent, on-site monitoring experience in a Pharmaceutical or Clinical Research Organisation - Our global Clinical Monitoring department consists of colleagues with institutional knowledge, in-depth therapeutic experience, and robust operational tools. Together, we help clients define and develop clinical programmes, minimise delays and execute high-quality, cost-efficient clinical studies. * Perform and coordinate all aspects of the clinical monitoring process. * Nationwide * Contract duration unspecified * Full Time - We are vital links between an idea for a new medicine and the people who need it.
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A strong scientific merit is required - must be perceived as a peer by the customer base (MD, PharmD., Pharmacist, PhD, advanced degree in medical or other life sciences) * Medical Experts (ME) Development and Management: Identify, develop, and collaborate with current and future thought leaders. * Medical Education and Communication: Educate ME, speakers, investigators and other external customers (e.g Hospital and other Health Committees) on novel and emerging data as per Scientific Operations and local business unit objectives/priorities. Foster medical and scientific information exchange between the medical community and our company. A strong scientific merit is required - must be perceived as a peer by the customer base (MD, PharmD., Pharmacist, PhD, advanced degree in medical or other life sciences) * Medical Experts (ME) Development and Management: Identify, develop, and collaborate with current and future thought leaders. * Medical Education and Communication: Educate ME, speakers, investigators and other external customers (e.g Hospital and other Health Committees) on novel and emerging data as per Scientific Operations and local business unit objectives/priorities. Foster medical and scientific information exchange between the medical community and our company.
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• Previous clinical research experience required. • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products. This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive relationships with colleagues within the Medical Devices Group. Responsible for managing clinical study activities for multiple sites in single or several clinical projects. Oversees performance of appointed study sites, conducting company initiated clinical studies. Serves as a member of the clinical study team and is the liaison between Clinical Operations and study site personnel for the specific clinical projects. Clinical Study Site Management consists 95% and other administrative activities 5%. • Previous clinical research experience required. • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products. This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive relationships with colleagues within the Medical Devices Group. Responsible for managing clinical study activities for multiple sites in single or several clinical projects. Oversees performance of appointed study sites, conducting company initiated clinical studies. Serves as a member of the clinical study team and is the liaison between Clinical Operations and study site personnel for the specific clinical projects. Clinical Study Site Management consists 95% and other administrative activities 5%.
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Inside Sales Representative Reproductive Health (m/f/d) The Inside Sales Representative will work to educate existing and prospective clinical facilities (hospitals and clinics) in Germany about the reproductive health portfolio and guide them through the process of adopting new medical technologies in their practice. DEPARTMENT: Sales / Business Development * Develop new customers in order to achieve or exceed sales objectives. * Utilize the CRM database to input and provide information that will increase effectiveness and aid sales. * Master's degree in natural sciences (biology, biochemistry, chemistry and biotechnology are preferred) with a proven academic and professional record, entry level experience in sales in healthcare products is helpful, but not a requirement. Jobs via StepStone.de * Hilden bei Düsseldorf * Contract duration unspecified * Full Time Inside Sales Representative Reproductive Health (m/f/d) The Inside Sales Representative will work to educate existing and prospective clinical facilities (hospitals and clinics) in Germany about the reproductive health portfolio and guide them through the process of adopting new medical technologies in their practice. DEPARTMENT: Sales / Business Development * Develop new customers in order to achieve or exceed sales objectives. * Utilize the CRM database to input and provide information that will increase effectiveness and aid sales. * Master's degree in natural sciences (biology, biochemistry, chemistry and biotechnology are preferred) with a proven academic and professional record, entry level experience in sales in healthcare products is helpful, but not a requirement. Jobs via StepStone.de * Hilden bei Düsseldorf * Contract duration unspecified * Full Time
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Senior Director, Medical Affairs - A fantastic opportunity has arisen within the MDx business area for the position of a Senior Director, Medical and Scientific Affairs. Jobs via StepStone.de * Hilden bei Düsseldorf * Contract duration unspecified * Full Time - At the heart of QIAGEN's business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe. Our most valuable asset are our employees – more than 5000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us. Senior Director, Medical Affairs - A fantastic opportunity has arisen within the MDx business area for the position of a Senior Director, Medical and Scientific Affairs. Jobs via StepStone.de * Hilden bei Düsseldorf * Contract duration unspecified * Full Time - At the heart of QIAGEN's business is a vision to make improvements in life possible. We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe. Our most valuable asset are our employees – more than 5000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us.
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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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In light of their further growth and professionalization we are looking for a Quality Assurance Officer IVD/Medical Devices. * 3 years of experience as a Quality Assurance Officer in a manufacturing environment, preferably in in-vitro diagnostics - In this role you are responsible for the maintenance and improvement of a robust Quality Management System (QMS) consistent with ISO 9001 and ISO 13485. * Management of quality tasks including change control, batch release and process validation * Participate in quality related investigations to resolve production, audit, and customer issues * Report and follow up on quality key performance indicators in a timely manner * Identify and support quality process improvements * Knowledge and practical application of Quality Management System ISO 13485, IVDD 98/79/EC, and In-Vitro Diagnostics Regulation (EU) 2017/746 is a plus - Motmans & Partners In light of their further growth and professionalization we are looking for a Quality Assurance Officer IVD/Medical Devices. * 3 years of experience as a Quality Assurance Officer in a manufacturing environment, preferably in in-vitro diagnostics - In this role you are responsible for the maintenance and improvement of a robust Quality Management System (QMS) consistent with ISO 9001 and ISO 13485. * Management of quality tasks including change control, batch release and process validation * Participate in quality related investigations to resolve production, audit, and customer issues * Report and follow up on quality key performance indicators in a timely manner * Identify and support quality process improvements * Knowledge and practical application of Quality Management System ISO 13485, IVDD 98/79/EC, and In-Vitro Diagnostics Regulation (EU) 2017/746 is a plus - Motmans & Partners
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The Country Trials Manager partners with the Study Start Up Project Manager, Study Manager, Site Intelligence Lead, Site Relationship Partner, Site Activation Partner, Contracts Lead, Regulatory Affairs, CRO representatives) and others as required. The Country Trials Manager is responsible for study startup deliverables for assigned studies at a country level that are of moderate to high complexity. For studies where there is more than one country trial manager assigned, may Country Trials Manager for the country or cluster of countries and coordinate all the country activities. The Country Trials Manager partners with the Study Start Up Project Manager, Study Manager, Site Intelligence Lead, Site Relationship Partner, Site Activation Partner, Contracts Lead, Regulatory Affairs, CRO representatives) and others as required. The Country Trials Manager is responsible for study startup deliverables for assigned studies at a country level that are of moderate to high complexity. For studies where there is more than one country trial manager assigned, may Country Trials Manager for the country or cluster of countries and coordinate all the country activities.
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The Country Trials Manager partners with the Study Start Up Project Manager, Study Manager, Site Intelligence Lead, Site Relationship Partner, Site Activation Partner, Contracts Lead, Regulatory Affairs, CRO representatives) and others as required. The Country Trials Manager is responsible for study startup deliverables for assigned studies at a country level that are of moderate to high complexity. For studies where there is more than one country trial manager assigned, may Country Trials Manager for the country or cluster of countries and coordinate all the country activities. The Country Trials Manager partners with the Study Start Up Project Manager, Study Manager, Site Intelligence Lead, Site Relationship Partner, Site Activation Partner, Contracts Lead, Regulatory Affairs, CRO representatives) and others as required. The Country Trials Manager is responsible for study startup deliverables for assigned studies at a country level that are of moderate to high complexity. For studies where there is more than one country trial manager assigned, may Country Trials Manager for the country or cluster of countries and coordinate all the country activities.
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The Translational Research operation manager is part of the TR department and serves as the HQ expert at practical implementation of TR and operationalize the policies and procedures that warrant quality of samples, sample processing, and sample analysis throughout trials. Do you want to act as the HQ expert at practical implementation of Translational Research and operationalize the policies and procedures that warrant quality of samples, sample processing, and sample analysis throughout trials and you're fluent in English? * Participates in the practical development and implementation of the TR part of protocol, being the interface between TR and clinical operation management. * Manage the portfolio of small projects using human biological material for translational research. The Translational Research operation manager is part of the TR department and serves as the HQ expert at practical implementation of TR and operationalize the policies and procedures that warrant quality of samples, sample processing, and sample analysis throughout trials. Do you want to act as the HQ expert at practical implementation of Translational Research and operationalize the policies and procedures that warrant quality of samples, sample processing, and sample analysis throughout trials and you're fluent in English? * Participates in the practical development and implementation of the TR part of protocol, being the interface between TR and clinical operation management. * Manage the portfolio of small projects using human biological material for translational research.
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Genomics Application Specialist - NGS and qPCR (m/f/d) To strengthen our Clinical Genomics and Genomics teams we are recruiting for a Genomics Applications Specialist who will primarily in Germany for NGS and PHC. The Genomics Applications Specialist will drive both pre-sales and post-sales activities for all NGS and PHC products in the defined territory according to the country action plans and ultimately supporting the sales of QIAGEN NGS and PHC solutions. From Liquid Biopsy and Oncology Biomarker Discovery to Metagenomics and Single Cell Sequencing, our application specific products in the genomics community. * Complete workflow support, product demonstrations, application consulting, workshops, on-site training and support, and support with technical queries including effective weekly/monthly planning of field based activities. Genomics Application Specialist - NGS and qPCR (m/f/d) To strengthen our Clinical Genomics and Genomics teams we are recruiting for a Genomics Applications Specialist who will primarily in Germany for NGS and PHC. The Genomics Applications Specialist will drive both pre-sales and post-sales activities for all NGS and PHC products in the defined territory according to the country action plans and ultimately supporting the sales of QIAGEN NGS and PHC solutions. From Liquid Biopsy and Oncology Biomarker Discovery to Metagenomics and Single Cell Sequencing, our application specific products in the genomics community. * Complete workflow support, product demonstrations, application consulting, workshops, on-site training and support, and support with technical queries including effective weekly/monthly planning of field based activities.
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This Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization. * Previous experience in clinical research or equivalent is desired * Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations * Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations * Support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones * Participate in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures This Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization. * Previous experience in clinical research or equivalent is desired * Good understanding of clinical research science and processes, clinical trends, and global clinical trial regulations * Proven track record in supporting clinical projects within clinical/ surgical research setting, on time, and in compliance to SOPs and regulations * Support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones * Participate in the feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures
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In your role as an Operations Manager you liaise with global affiliate offices and their project managers on behalf of Notified Body 1639. Ultimately, a successful Operations Manager should ensure the efficient and smooth day-to-day operation of our office but also keep a keen eye on adhering to procedures and standards. We are currently looking for an Operations Manager for the SGS Notified Body 1639 in Antwerp. As our Operations Manager you implement and improve our certification procedures. Our ideal new colleague has a proven experience as an Operations Manager and is analytic and critical in observation, yet capable of implement findings in improvement plans based on forecasting. In this role as an Operations Manager you are fluent in English and Dutch (any other EU language is an asset) In your role as an Operations Manager you liaise with global affiliate offices and their project managers on behalf of Notified Body 1639. Ultimately, a successful Operations Manager should ensure the efficient and smooth day-to-day operation of our office but also keep a keen eye on adhering to procedures and standards. We are currently looking for an Operations Manager for the SGS Notified Body 1639 in Antwerp. As our Operations Manager you implement and improve our certification procedures. Our ideal new colleague has a proven experience as an Operations Manager and is analytic and critical in observation, yet capable of implement findings in improvement plans based on forecasting. In this role as an Operations Manager you are fluent in English and Dutch (any other EU language is an asset)
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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 * 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 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 * 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?
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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 looking for a Product Support Technician co-dev who will technically and administratively support in the manufacturing clinical supplies. Through a personal follow-up, you receive quality support in every step that you accommodate. Jefferson Wells * Puurs * Contract duration specified,Freelance * Full Time - Our partner innovates to bring treatments to patients that significantly improve their lives. Together with the government and other health partners, they work on high-quality, affordable and accessible healthcare.  Your responsibilities - You have a scientific degree (Bachelor or Master) with a couple of years' experiences in a technical/ scientific area. You have good communication skills both written and spoken in Dutch and English. You have experience in pharmaceutical industry. You work organized, you are proactive, accurate and a team player. Your profile - Will you be our new ambassador? We are looking for a Product Support Technician co-dev who will technically and administratively support in the manufacturing clinical supplies. Through a personal follow-up, you receive quality support in every step that you accommodate. Jefferson Wells * Puurs * Contract duration specified,Freelance * Full Time - Our partner innovates to bring treatments to patients that significantly improve their lives. Together with the government and other health partners, they work on high-quality, affordable and accessible healthcare.  Your responsibilities - You have a scientific degree (Bachelor or Master) with a couple of years' experiences in a technical/ scientific area. You have good communication skills both written and spoken in Dutch and English. You have experience in pharmaceutical industry. You work organized, you are proactive, accurate and a team player. Your profile - Will you be our new ambassador?
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PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose - to improve health! Envision a workplace where you have a direct impact on improving health, , use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD® Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success. PPD is currently recruiting for a Medical Technologist to join our Central Laboratory in Zaventem, Brussels. * Zaventem * Contract duration unspecified * Full Time - PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose - to improve health! Envision a workplace where you have a direct impact on improving health, , use newest technologies and collaborate with industry thought leaders and therapeutic experts. Welcome to PPD® Laboratories, where science is our passion, quality is our commitment and people are the cornerstone of our success.
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To strengthen their growing organization, they are looking for a « Clinical Trial Assistant » (F/M). (CMO), you will ensure the administrative and logistics management of the clinical trials, what includes their implementation, follow-up and closure in * Notions of clinical trial administrative management ; Or do have a first administrative experience in the clinical research? With its strong portfolio of clinical programs (Phase II and Phase III) and preclinical programs, our client is organized as a "mini-pharma", with departments for preclinical - research, clinical studies, production, quality control, quality assurance, regulation and administration. compliance with the regulations in force, Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs). * Updating and maintaining documentation and ensuring the traceability of documents related to clinical development ; To strengthen their growing organization, they are looking for a « Clinical Trial Assistant » (F/M). (CMO), you will ensure the administrative and logistics management of the clinical trials, what includes their implementation, follow-up and closure in * Notions of clinical trial administrative management ; Or do have a first administrative experience in the clinical research? With its strong portfolio of clinical programs (Phase II and Phase III) and preclinical programs, our client is organized as a "mini-pharma", with departments for preclinical - research, clinical studies, production, quality control, quality assurance, regulation and administration. compliance with the regulations in force, Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs). * Updating and maintaining documentation and ensuring the traceability of documents related to clinical development ;
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• Previous clinical research experience required. • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products. This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive relationships with colleagues within the Medical Devices Group. Responsible for managing clinical study activities for multiple sites in single or several clinical projects. Oversees performance of appointed study sites, conducting company initiated clinical studies. Serves as a member of the clinical study team and is the liaison between Clinical Operations and study site personnel for the specific clinical projects. Clinical Study Site Management consists 95% and other administrative activities 5%. • Previous clinical research experience required. • Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products. This individual will be responsible for managing clinical activities at study sites conducting studies for the Medical Devices group, as well as, fostering strong, productive relationships with colleagues within the Medical Devices Group. Responsible for managing clinical study activities for multiple sites in single or several clinical projects. Oversees performance of appointed study sites, conducting company initiated clinical studies. Serves as a member of the clinical study team and is the liaison between Clinical Operations and study site personnel for the specific clinical projects. Clinical Study Site Management consists 95% and other administrative activities 5%.
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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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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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