My client is a global CRO currently in need of a number of UK based Freelance Clinical SAS Programmers. In line with their ongoing sponsor driven work my client are looking for up to five programmers to join them on initial 6 month contracts. By working on various studies, they are able to provide a diverse and interesting workload as well as the flexibility to work from home in the UK. ...
My client are a global CRO who are currently working on an exciting and varied range of projects for a large number of Pharmaceutical sponsors. With offices in several countries in Europe they are currently in the process of looking for experienced SAS programmers (office based and home based) to join them on a contract basis. ...
I am working with a global organisation in the Pharmaceutical industry who is looking for a SAS Programmer to join their team West of London on a 6 months contract. You will need to be available at relatively short notice and have extensive industry experience
The Statistical Programmer provides technical expertise for the conduct of clinical trials
The SAS Statistical Programmer (CP) will be responsible for accessing and gathering clinical data from an array of sources, reorganising the data to tabulation datasets and building derived datasets adhering to industry and client stipulations
Our client is a leading international CRO providing comprehensive drug development capabilities worldwide. They require an experienced Senior Statistical Programmer to lead their Statistical Programming team.
SEC Pharma is working in close collaboration with a leading clinical services company in recruiting for a Manager, Statistical Programming for their offices in London. You will be responsible for a senior team, ensuring the successful delivery of project deliverables. As an experienced leader, you will work independently and report directly to Senior Directors. ...
Our client is looking for an experienced SDTM Programmer to provide support for mapping and transformation of clinical data to CDISC SDTM standards. You will be responsible for extracting data and mapping the data from an in house standard to industry standard.
You will need SDTM expertise which will cover the core SDTM standards, aCRF, define.xml. SAS Programming(to check complicated conversions) and lastly Project Management skills as you will be managing up to 7 studies at a time.
Our client is looking for a Statistician or Senior Statistician to join a European team within late phase and real world; this is an exciting time to join a growing team. The successful candidate will have a working knowledge of statistical methods used for clinical trials and observational studies and will be experienced in using SAS. The role comes with a negotiable salary and excellent benefits.
Our client is looking for a Statistician or Senior Statistician to join a new European team within late phase and real world. The successful candidate will have a working knowledge of statistical methods used for clinical trials and observational studies and will be experienced in using SAS. The role comes with a negotiable salary and excellent benefits.
I am currently seeking a Senior Biostatistician for a leading organisation to take responsibility for the statistical element of international projects. The individual in this role will be seen as the go to person for other colleagues and the companies’ clients for all assistance required related to Biostatistics. The Senior Biostatistician will need to have worked within a consulting environment, sitting within the Health Economics & Outcomes Research team
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