Job DescriptionSenior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming)\nThe Role\nCSL is looking for a Senior Programmer to take technical ownership of one or two clinical t...Read More>>.

Overview In this role you drive statistical programming for clinical trials, acting as a technical SME and, when needed, leading programming on projects. You collaborate with sponsors and cross-functional teams to ensure quality, timelines,...Read More>>.

Overview In this SAS Programmer role, you contribute to the clinical data analysis by building analysis datasets, tables, listings, and figures. You will work within the Clinical Database Programming & Biostatistics team to program, validat...Read More>>.

Overview In this role you will join the Data Management team in London to design and maintain clinical study EDC databases that support analysis and reporting. You’ll work with data managers and project teams to deliver timely, quality da...Read More>>.

Overview In this role you will own data management across the full trial lifecycle, working with EDC systems to support complex clinical studies. You will develop and maintain data validation, QC, and reporting scripts to enable clear trial...Read More>>.

Senior Clinical Statistical Programmer (Portfolio Development / Biometrics / Programming) The RoleCSL is looking for a Senior Programmer to take technical ownership of one or two clinical trials from first line...Read More>>.

A leading global CRO is seeking a Senior Statistical Programmer for a permanent home-based position. The role involves designing data structures, ensuring the quality of clinical data submissions, and leading programming activities across multiple st...Read More>>.

A global clinical research organization in London is inviting applications for a SAS Programmer role. This position requires a Bachelor's degree in relevant fields and SAS Base Certification. Responsibilities include writing SAS programs, validating...Read More>>.

A clinical research organization is looking for a SAS Programmer III with strong SAS and R skills to support clinical trials remotely in the UK. The role involves programming SDTM and ADaM datasets, performing quality control, and collaborating with...Read More>>.

A leading pharmaceutical company is seeking a Senior Principal Statistical Programmer to lead RWE projects and develop R Shiny applications. This full-time remote role requires expertise in R and SAS, with a focus on delivering decision-ready insight...Read More>>.

Place2Be is looking for an experienced and passionate Clinical Programme Lead to join our Mental Health Workforce Development team, playing a pivotal role in shaping the future children and young people’s Mental Health. This role leads the cl...Read More>>.

Place2Be is seeking a Clinical Programme Lead in Greater London to guide the clinical delivery of training programmes for children's mental health. This role involves ensuring curriculum quality, overseeing delivery, and supporting trainers, while...Read More>>.

Medpace is expanding its Clinical Informatics team and seeks qualified individuals to support data analytics, visualization, and accessibility across studies. You will work with Clinical Operation teams to develop data products, primarily Shiny ap...Read More>>.

Worldwide Clinical Trials is seeking an experienced Biostatistician to join our UK team. You will lead statistical aspects of clinical studies, design analyses, specify listings and tables, and provide expert consultancy to sponsors and study team...Read More>>.

Job SummaryDue to our continued growth, we are in need of qualified and focused driven individuals for SAS Programmer role to be office-based in Stirling, UK. This is a vital role in our Clinical Database Programming & Biostatistics depar...Read More>>.

Veramed is seeking a Data Management Programmer to join a sponsor-dedicated team, working as a fully integrated member of a global Data Management Programming function. The role focuses on generating Data Management listings from raw clinical tria...Read More>>.

CSL Vifor in Maidenhead seeks a Senior Clinical Statistical Programmer to own one or two trials from first line of code to submission-ready package. You will design, validate SDTM/ADaM datasets and outputs, work with statisticians and data manager...Read More>>.

St Bartholomew's Hospital is building a vibrant, ambitious nursing and allied professional (NAP) research culture. We are committed to ensuring every NAP role includes research. We are seeking an enthusiastic and motivated Clinical Research Pro...Read More>>.

Johnson & Johnson in Buckinghamshire, United Kingdom, seeks an Experienced Statistical Programmer who supports the analysis and reporting of clinical data within the Statistical Programming team. You will apply statistical programming methods, ens...Read More>>.

Parexel in the United Kingdom is seeking a Senior Statistical (SAS) Programmer to join our FSP team. The role provides technical expertise for the conduct of clinical trials, supports analysis and reporting of study data, and may assume the Statis...Read More>>.

Parexel is seeking a Senior Statistical (SAS) Programmer to join our FSP team in the UK, Hungary, Poland or Serbia. The role provides technical expertise for clinical trial analysis and reporting, acting as an internal SME and supporting programmi...Read More>>.

Parexel is looking for a Senior Statistical (SAS) Programmer to join our FSP team in either the UK, Hungary, Poland or SerbiaThe Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as a...Read More>>.

Syneos Health in the United Kingdom is seeking a Principal Statistical Programmer to lead sponsor-dedicated programming efforts. The role supports remote work for UK or South Africa, with responsibilities across SAP-driven outputs and regulatory c...Read More>>.

Experis Austria seeks a Programme Manager to lead a large-scale global data migration initiative for a banking client, based in Sheffield with hybrid working. You will shape the delivery strategy, engage senior stakeholders and ensure delivery fro...Read More>>.

Johnson & Johnson in High Wycombe, United Kingdom, seeks an Experienced Statistical Programmer to support data analysis and reporting for clinical studies. You will develop, verify, and document code for analysis and reporting, ensuring timely and...Read More>>.

Roche Products Ltd. in Welwyn is seeking an Analytical Data Science Programmer to transform statistical analysis plans into high-quality, traceable programming outputs for clinical studies.This role involves creating SDTM/ADaM datasets, tab...Read More>>.

Key InformationSalary: Salary from £61,189 per annum. Commencement on the salary range is subject to comparable skills and experience. Future progression is based on annual performance review.Duration of Contract: Fixed Term for 2...Read More>>.

The Institute of Cancer Research is seeking an experienced trialist to join the Cancer Research UK Clinical Trials & Statistics Unit (ICR-CTSU) as a Clinical Trials Programme Manager at its Sutton site in Surrey. The role involves leading multi-ce...Read More>>.

Amgen, a leading biotechnology company, invites placement students to join the Biostatistics department in Cambridge or Uxbridge for up to ten months. You will gain experience in SAS/R programming, analyzing and interpreting clinical trial data, a...Read More>>.

Johnson & Johnson Innovation is seeking an Experienced Clinical Programmer to lead complex clinical data tasks and support SDTM submissions. You will oversee data management activities, create edit checks, and develop study-specific reports to mon...Read More>>.

Cytel invites Senior Statistical Programmers to join a sponsor-dedicated program, working fully embedded with a pharmaceutical client while Cytel supports from behind the scenes. You will leverage advanced SAS and CDISC SDTM/ADaM skills to support...Read More>>.

Roche in the United Kingdom is seeking an Analytical Data Science Programmer to transform statistical analysis plans into high-quality, traceable programming outputs for clinical studies, including TLFs, datasets (SDTM/ADaM), and interactive visua...Read More>>.

MMS is seeking a Senior Biostatistician to join our data-focused CRO. You will lead biostatistical deliverables across trials, collaborate with sponsors and cross-functional teams, and ensure high-quality analyses aligned with CDISC standards and...Read More>>.

Parexel International is seeking a Senior Statistical Programmer to join our FSP team across the UK, Hungary, Poland, or Serbia. The role involves technical leadership in statistical programming for clinical trials, ensuring quality, timelines, bu...Read More>>.

The Institute of Cancer Research in Sutton, Surrey, is seeking an experienced Clinical Trials Programme Manager to join the ICR-CTSU Management Group. You will oversee a defined portfolio and drive initiation of new trials across multi-centre site...Read More>>.

Celerion is seeking a full-time Biostatistician for our Data Management and Biometric department in the United Kingdom. You will develop statistical analysis plans, perform SAS-based analyses, and prepare reports for assigned projects, contributin...Read More>>.

Bristol Myers Squibb in the UK is seeking a Senior Statistical Programmer to join our GBDS function. You will own your programming workload with real autonomy, delivering high-quality SAS-driven analyses that support regulatory submissions....Read More>>.

Thrive IT Systems is seeking a senior transformation leader to direct large-scale platform and data migration programmes across multiple workstreams and geographies. You will own governance, roadmaps, and delivery assurance, coordinating across bu...Read More>>.