Statistical programmer jobs in WiganCreate job alerts

Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes. Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge. 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. We can offer home and/or office working, training and support and a competitive package. The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.g. line management and/or project management). Key Responsibilities Technical • Previous experience with SAS and R., • Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs, • Author, review and approve study TFL shells and dataset specifications, • Author, validate and document SAS programs for datasets, TFLs and macros, applying good programming practice • Identify data issues and outliers, • Complete, review and approve CDISC Validation tool reports, • Identify data and standards issues and resolve or escalate as appropriate, • Awareness of emerging standards and associated impact to ongoing and future planned trials, • Maintain proficiency in SAS and awareness of developments, • Maintain study master file documents and any other documents that are required to be audit ready General • Lead internal and client study, project and cross functional team meetings effectively, • Present study updates internally and at client meetings, • Share scientific, technical and practical knowledge within the team and with colleagues, • Perform work in full compliance with applicable internal and client policies, procedures, processes and training • Build effective collaborative working relationships with internal and client team members, • Ensure learnings are shared across projects or studies, • Develop and provide internal technical training where appropriate, • Lead process improvement initiatives Minimum Qualification Requirements • BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience), • At least 6 years of relevant industry experience Other Information/ Additional Requirements • Understanding of clinical drug development process, relevant disease areas, endpoints and study designs WHAT TO EXPECT: • A warm, friendly working environment in which to thrive both personally and professionally., • A supportive, open-door management policy that will aid in your development and provide you with the tools to take your career to the next level., • A truly unique CRO that’s doing something different when it comes to managing staff, projects and building relationships in the industry., • The ability to own your role and develop your skills and experience.

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

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.

World leading CRO recently awarded Best Employer have a new opportunity for a Principal Statistical Programmer to join their FSP Team. 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

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

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

Senior Statistical Programmer (UK Remote). We are looking for an experienced statistical programmer to join our remote team. Program and validate statistical analyses of clinical studies with SAS.

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

A leading pharmaceutical company in Greater London is seeking a Principal Statistical Programmer to lead statistical programming activities for clinical studies.

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. At least 8 years of experience in clinical trial statistical programming.

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.

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

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

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

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

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

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

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

A leading pharmaceutical company is seeking a Senior Principal Programmer to lead statistical programming tasks for clinical studies. This role requires deep expertise in SAS and statistical analysis, along with the ability to coordinate internal and external programming teams.

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

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,

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.

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. Program customized data displays, (including data listings, summary tables and routine g

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

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 clinical research company is seeking an experienced Senior Statistical Programmer to join their remote team in the UK. The role involves programming, validation, and quality control of statistical analyses for clinical studies using SAS.

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

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

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. Statistical Programmer o

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

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. The Principal Statistica

A leading biostatistics firm is searching for a Principal Statistical Programmer to work with a global pharmaceutical client in London. Responsibilities include overseeing CRO programmers, preparing regulatory submissions, and ensuring high-quality deliverables.

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 (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.

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

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

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.

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

SwitzerlandLondon (The Westworks), United KingdomREQ-10070499### Senior Principal Statistical ProgrammerREQ-10070499### Senior Principal Statistical Programmer #J-18808-Ljbffr. About the RoleKey Accountabilities:* Lead statistical programming activities as Trial Programmer for several studies or

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

United KingdomREQ-10070390### Principal Statistical ProgrammerREQ-10070390### Principal Statistical Programmer #J-18808-Ljbffr. About the RoleKey Accountabilities:* Lead statistical programming activities as Trial Programmer for either a large/pivotal study or several studies, or act as a Lead/P

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