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A leading healthcare data company in Greater London is seeking a Senior Statistical Programmer with expertise in SAS programming and clinical trial data management. The ideal candidate has a Master's degree in Statistics and a minimum of 5 years' experience in statistical programming.

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. You program and validate statistical analysis of clinical studies with SAS.

A leading global research organization is seeking a Senior Statistical Programmer in Greater London. Ideal candidates have a BSc in relevant fields and at least 5 years of statistical programming experience, particularly in a CRO/pharmaceutical environment.

United KingdomREQ-10070390### Principal Statistical ProgrammerREQ-10070390### Principal Statistical Programmer #J-18808-Ljbffr. Your experience:*** BA/BS/MS or international equivalent experience in statistics, computer science, mathematics, life sciences or related field* Experience in a programmin

A pioneering healthcare company is seeking a Lead Statistical Programmer to enhance oncology care through data analysis. The role involves translating statistical plans into analytic solutions, mentoring junior staff, and collaborating on research projects.

A leading pharmaceutical company in Greater London is seeking a Senior Principal Statistical Programmer. The ideal candidate will have strong SAS expertise and experience in statistical analysis within clinical trials. This role will lead statistical programming activities for clinical studies, ensu

Principal Statistical Programmer (US, CAD, UK only). Acts as the lead statistical programmer. Participates in sponsor meetings, kickoff meetings, and bid defense meetings as statistical programming representative, as required by sponsor.

A leading pharmaceutical company is seeking a Principal Statistical Programmer in the United Kingdom. The role involves leading statistical programming activities for pivotal studies, ensuring timely and high-quality deliverables.

A leading healthcare organization in Greater London is seeking a Principal Statistical Programmer responsible for all aspects of statistical programming for pivotal studies.

Principal Statistical Programmer (US, CAD, UK only). Acts as the lead statistical programmer. Uses SAS or other software to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specificati

A global healthcare company is seeking a Senior Principal Statistical Programmer to lead statistical programming activities for clinical studies.

The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Leads and ove

We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. Statistical Programmer o

Senior Statistical Programmer (contract). The Senior Statistical Programmer will contribute expert programming skills to deliver accurate, regulatory-compliant clinical data outputs for Compass Pathways development programs. Reviewing of the Statistical Analysis Plan (SAP) and shells.

A leading global CRO is seeking a Senior Statistical Programmer for a permanent home-based position.

SwitzerlandLondon (The Westworks), United KingdomREQ-10070499### Senior Principal Statistical ProgrammerREQ-10070499### Senior Principal Statistical Programmer #J-18808-Ljbffr. Your experience:*** BA/BS/MS or international equivalent experience in statistics, computer science, mathematics, life scie

A clinical research organization in the UK seeks a Principal or Senior Statistical Programmer skilled in SAS and R.

A leading biopharmaceutical solutions organization is seeking a Principal Statistical Programmer located in the UK. You will leverage significant experience in ADaM specification writing and SAS programming to ensure the integrity of statistical outputs. The role involves leading statistical program

We have an exciting opportunity for a Principal or Senior level Statistical Programmer skilled in SAS & R to join us on a permanent basis in the UK. The Senior or Principal Programmer may also perform a supervisory role (e.

Get notified about new Statistical Programmer jobs in. Clinical Programmer (SCP) plays a pivotal role in supporting clinical research by developing, validating, and maintaining statistical programs and datasets. Collaborating with Biostatisticians, Clinical Data Managers, and cross-functional teams,

Senior Statistical Programmer Consultant. Works proactively with study team members including but not limited to the Statistician, Lead Programmer, Data Manager and Study Leader. Implements statistical programming aspects of the protocol and the clinical development program.

A biotechnology company is seeking a Senior Statistical Programmer for a fixed-term contract of 9 months. The ideal candidate will have extensive statistical programming experience, knowledge of regulatory submissions, and proficient skills in SAS and R.

A leading global CRO is seeking a Senior Statistical Programmer Consultant to support clinical projects. This role requires strong statistical programming skills and experience in oncology.

A global biostatistics and programming company is seeking a Principal Statistical Programmer to work embedded with one of their pharmaceutical clients in the UK.

A leading biopharmaceutical solutions organization is seeking a Principal Statistical Programmer in the UK. The role involves developing statistical programming, ensuring quality outputs, and mentoring junior staff.

Act as a shadow lead programmer and attend customer meetings alongside the Lead Programmer as required. We are looking for a SAS Programmer III who can also program in R with a background in working across clinical trials, ideally with experience in oncology. You will work closely with programmers,

Develop SAS programming codes to independently validate statistical output reports of trial data generated by other programmers or statisticians. Provide technical guidance and support to less experienced Statistical Programmers. These designs and specifications are completed in accordance with comm

Lead statistical programming activities as Trial Programmer for several studies or as Lead/Program Programmer for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization. Experience as Trial/Lead/Project Programmer for several studies or project�

Senior Statistical Programmer | Independent CRO | Home Based | UK |. We’re seeking elite Senior Statistical Programmers to join this growing organisation remotely from anywhere in the UK. If this opportunity is of interest, please apply now with your CV as the organisation are looking to arrange i

Perform quality control checks of advanced SAS code for datasets and output produced by other statistical programmers.

If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Principal Statistical Programmer onboard as soon as possible. World leading CRO recently awarded Best Employer have a new opportunity for a Principal Statistical Programmer to join th

Lead statistical programming activities as Trial Programmer for either a large/pivotal study or several studies, or act as a Lead/Program Programmer for a small to medium sized project in phase I to IV clinical studies in Novartis Global Drug Development. The Principal Statistical Programmer is resp

Senior Principal Statistical Programmer (RWE). Senior Principal Statistical Programmer. This role involves leading statistical programming for real-world data (RWD) projects and developing interactive applications to support decision-making, regulatory, and HTA submissions.

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