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Senior/Principal Statistical Programmer Consultant. Senior/Principal Statistical Programmer Consultant. Senior/Principal Statistical Programmer Consultant.

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.

A global full-service CRO is seeking a Senior/Principal Statistical Programmer Consultant in the United Kingdom.

A leading clinical research organization in the UK is seeking a Principal or Senior Statistical Programmer to provide programming support across various projects.

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. Join to apply for the Pr

Principal or Senior Statistical Programmer – Remote, Office or Hybrid – UK. The Principal or Senior Statistical Programmer will provide programming support across a range of projects, clients and therapeutic areas, and may assume supervisory roles.

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,

A global contract research organization is looking for a Senior/Principal Statistical Programmer Consultant to oversee programming efforts for clinical studies.

A leading biopharmaceutical company based in the UK is seeking a Principal Statistical Programmer to play a key role in their clinical development programs.

A leading health outcomes consultancy seeks a Statistical Programmer to analyze patient-reported outcome data from clinical trials. You will contribute to high-quality statistical analysis and collaborate within a dynamic team. Essential qualifications include SAS Base Certification and a graduate d

At least 2+ years of trial lead experience preferably as the lead for a team of programmers OR At least 2+ years of experience developing SAS/R solutions that are implemented broadly across clinical programs or a therapeutic area.

Get notified about new Senior Statistical Programmer jobs in. Senior Statistical Programmer (FSP - Permanent Homebased). Senior Statistical Programmer (FSP - Permanent Homebased).

Principal Statistical Programmer | Leading CRO | Home Based | UK. We are seeking experienced Principal Statistical Programmers to join remotely from anywhere in the UK. Lead statistical programming projects, ensuring high-quality, on-time deliverables.

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

A clinical research firm is looking for a Senior/Principal Statistical Programmer to manage clinical trial data in the UK.

Tools & Standards Senior Specialist/Statistical Programmer with R (FSP). The Tools and Standards Specialist will have a background in Statistical Programming using R and (desirably) SAS as well as experience participating and leading in standardization and automation. Job Category Statistical Progra

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�

A leading consultancy in clinical programming is seeking a Principal Statistical Programmer with a strong background in oncology studies. You will be involved in generating specifications, developing statistical programs using SAS, and overseeing CRO deliverables to meet high-quality standards. This

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. Responsible for quality control and audit readiness of all assigned statist

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. As a Principal Statistic

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

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. As a Principal Statistic

Contract Senior / Principal Statistical Programmer – UK (Remote). We have exciting Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work with Veramed. Familiarisation with simple statistical techniques (e.

We are looking for Senior Statistical Programmers in the UK to join Veramed, where you'll deliver high-impact programming solutions in an FSP-style capacity, while advancing your career in a supportive, growth-driven environment. As a Senior Statistical Programmer at Veramed, you'll have varied resp

If this opportunity is of interest, please apply now with your CV as the organisation are looking to arrange interviews for the Statistical Programmers as soon as possible. Get notified about new Statistical Programmer jobs in. Senior Statistical Programmer 1 - UK/EU - Remote.

A global pharmaceutical company is seeking a Principal Statistical Programmer to work embedded within a major client. The role focuses on delivering high-quality statistical programming, managing CRO deliverables, and ensuring adherence to FDA regulations.

A leading healthcare organization in Greater London seeks a Senior Principal Programmer to lead statistical programming for clinical trials.

A leading statistical programming firm in the UK is seeking a Senior Statistical Programmer to join their team.

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

The Tools and Standards Specialist will have a background in Statistical Programming using R and (desirably) SAS as well as experience participating and leading in standardization and automation.

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

Senior/Principal Statistical Programmer Consultant. The Senior/Principal Statistical Programmer Consultant is a delivery-focused role who works under the leadership, oversight, and direction of a Programming team leader to lead and/or support aspects of the programming effort to deliver technical pr

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

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. Develop SAS programming codes and generate complete and accurate stati

A leading health outcomes consultancy is seeking a Statistical Programmer to analyze patient-reported outcome data for clinical trials and psychometric studies. The role involves data manipulation, statistical analysis, and creating SAS programs.

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.

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