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Clinical research: Opportunities at SGS

Clinical research: Opportunities at SGS

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In the spirit of continued growth and to help improve our business, we are seeking candidates for the following position (m/f): Application developer...

014330 Requisition #

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We are recruiting for our International Project Management team in our Belgian offices and are currently seeking to hire a Clinical Project Manager...

014772 Requisition #

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SGS is the world’s leading inspection, verification, testing and certification company. The company employs over 86.000 people and operates a network of more than 1000 offices and laboratories around the world. One of the business segments, Clinical research, is a leading Contract Research Organization (CRO) providing drug development and post-approval services to the pharmaceutical and biopharmaceutical industry. It’s Biostatistics department is strongly expanding and therefore looking for several new colleagues in the position of : Senior Biostatisticians – Candidates can work office based in Belgium (Mechelen) or home based in Spain, Germany, the UK, the Netherlands In this position you will be responsible for the generation, validation and communication of the statistical results for multiple clinical research projects in a wide variety of therapeutic areas. Able to work independently and collaboratively, your primary responsibilities will include: • Participate in building the design of a clinical trial protocol, with inclusion of sample size calculation • Write and review the statistical analysis plan for phase I to IV trials • Develop Table Shells and specifications on CDISC ADaM datasets • Program and validate the statistical analysis, possibly in co-operation with other Biostatisticians and/or Statistical Programmers • Pay special attention to the inferential statistics with inclusion of thorough quality control by double programming • Communicate to the Data Manager on database topics to guarantee reliable conclusions • Create high-quality graphs for visualization of data and analytic results • Review the Clinical Study Report and support the Medical Writer in the interpretation of the statistical results • Work in close collaboration with the Biostatistical Coordinator and other colleagues

017860 Requisition #

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SGS is the world’s leading inspection, verification, testing and certification company. The company employs over 86.000 people and operates a network of more than 1000 offices and laboratories around the world. One of the business segments, Clinical research, is a leading Contract Research Organization (CRO) providing drug development and post-approval services to the pharmaceutical and biopharmaceutical industry. It’s Biostatistics department is strongly expanding and therefore looking for several new colleagues in the position of Senior Statistical Programmer Candidates can work office based in Belgium (Mechelen) OR home based in Spain, Germany, the UK, the Netherlands In this position you will be responsible for the generation and communication of the statistical results for multiple clinical research projects in a wide variety of therapeutic areas. Able to work independently and collaboratively, your primary responsibilities will include: • Participate in building the design of a clinical trial phase I protocol • Write and review the statistical analysis plan for phase I trials • Develop Table Shells and specifications on CDISC ADaM datasets • Program and validate the statistical analysis, possibly in co-operation with other Biostatisticians and/or Statistical Programmers • Communicate to the Data Manager on database topics to guarantee reliable conclusions • Create high-quality graphs for visualization of data and analytic results • Work in close collaboration with the Biostatistical Coordinator and other colleagues

017708 Requisition #

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SGS is the world’s leading inspection, verification, testing and certification company. The company employs over 86.000 people and operates a network of more than 1000 offices and laboratories around the world. One of the business segments, Clinical research, is a leading Contract Research Organization (CRO) providing drug development and post-approval services to the pharmaceutical and biopharmaceutical industry. It’s Biostatistics department is strongly expanding and therefore looking for several new colleagues in the position of : Senior Statistical Programmers - Candidates can work office based in Belgium (Mechelen) or home based in Spain, Germany, the UK, the Netherlands In this position you will be responsible for the generation and communication of the statistical results for multiple clinical research projects in a wide variety of therapeutic areas. Able to work independently and collaboratively, your primary responsibilities will include: • Participate in building the design of a clinical trial phase I protocol • Write and review the statistical analysis plan for phase I trials • Develop Table Shells and specifications on CDISC ADaM datasets • Program and validate the statistical analysis, possibly in co-operation with other Biostatisticians and/or Statistical Programmers • Communicate to the Data Manager on database topics to guarantee reliable conclusions • Create high-quality graphs for visualization of data and analytic results • Work in close collaboration with the Biostatistical Coordinator and other colleagues

017861 Requisition #

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SGS is the world’s leading inspection, verification, testing and certification company. The company employs over 86.000 people and operates a network of more than 1000 offices and laboratories around the world. One of the business segments, Clinical research, is a leading Contract Research Organization (CRO) providing drug development and post-approval services to the pharmaceutical and biopharmaceutical industry. It’s Biostatistics department is strongly expanding and therefore looking for several new colleagues in the position of : Senior Biostatisticians – Candidates can work office based in Belgium (Mechelen) or home based in Spain, Germany, the UK, the Netherlands In this position you will be responsible for the generation, validation and communication of the statistical results for multiple clinical research projects in a wide variety of therapeutic areas. Able to work independently and collaboratively, your primary responsibilities will include: • Participate in building the design of a clinical trial protocol, with inclusion of sample size calculation • Write and review the statistical analysis plan for phase I to IV trials • Develop Table Shells and specifications on CDISC ADaM datasets • Program and validate the statistical analysis, possibly in co-operation with other Biostatisticians and/or Statistical Programmers • Pay special attention to the inferential statistics with inclusion of thorough quality control by double programming • Communicate to the Data Manager on database topics to guarantee reliable conclusions • Create high-quality graphs for visualization of data and analytic results • Review the Clinical Study Report and support the Medical Writer in the interpretation of the statistical results • Work in close collaboration with the Biostatistical Coordinator and other colleagues

017709 Requisition #

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