11 of 11 DemandTrendPermanent Statistical Programmer Jobs in the UK

Principal, Statistical Programmer page is loaded Principal, Statistical Programmer Apply remote type: Remote locations: Europe-Remote, London-Remote; time type: Full time; posted on: Posted Yesterday; job requisition id: JR000430 Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you. … ideas are explored with an open mind, driven by our shared values: be courageous, be accountable, be honest, be inclusive, and elevate others. Job Description Summary Support and lead statistical programming activities on client clinical projects, including complex projects, producing high-quality deliverables on time and following relevant SOPs. Job Description Role The Principal Statistical Programmer will … support and lead statistical programming activities on client clinical projects, including complex projects. They will produce high-quality deliverables within agreed timelines and follow SOPs. Additionally, they will support effective deployment of project resources and contribute to maintaining an efficient statistical programming department. Key Responsibilities Lead statistical programming activities on clinical projects, including complex projects. Support the More ❯

Senior Statistical Programmer (Remote - Permanent Homebased) page is loaded Senior Statistical Programmer (Remote - Permanent Homebased) Apply locations Reading, Berkshire, United Kingdom Solna, Sweden Paris, France Copenhagen, Denmark Gothenburg, Sweden time type Full time posted on Posted Yesterday job requisition id R Why IQVIA This role will be dedicated to one of IQVIA's largest clients through … a collaborative approach to study work Variety of therapeutic areas, indications and, study phases Job stability; long-term engagements and development opportunities Career advancement opportunities Job Description The Senior Statistical Programmer will be responsible for review datasets in submission ready standard format (ADaM), tables, figures, listings and submission packages. This individual will provide expertise in the design, development … to analyze and report complex clinical trial data in CDISC ADaM format. Leads and oversees the development of global tools that will increase the efficiency and capacity of the Statistical Programming group. Works closely with clinical study teams to plans and executes activities to ensure project timelines are met with high quality deliverables. Additional tasks: • Collaborates with CR&D More ❯

We are in search of a Senior Principal Statistical Programmer, with expertise in HTA and Pricing and Reimbursement activities. This role offers the chance to provide statistical programming solutions to HTA problems. The successful candidate will work closely with International Value & Access and HEOR teams to shape ways of working for Joint Clinical Assessment in Europe to … ensure high-quality deliverables. The Senior Principal Statistical Programmer will be responsible for all statistical programming aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high-quality deliverables. Complies with project/… study standards and specifications following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. About the Role Key requirements Lead statistical programming activities for a medium to large sized project in phase I to IV clinical studies in Novartis Global Development Organization. Co-ordinate activities of programmers either internally or externally. Make statistical More ❯

culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients. Responsibilities You will be responsible for completion of the following: Create, validate, execute and generate statistical … planning Tracking and work allocation to ensure project, timeline and quality goals are consistently achieved. Additionally, you will contribute to the review and quality control of programming deliverables, including statistical programs and supporting specifications and documentation. You will effectively liaise with other functions in the conduct of programming activities and support other project activities such as addressing audit findings … strong communicator with a proactive nature and a willingness to work as part of a team A minimum of 5 years relevant experience of successfully performing the role of Statistical Programmer, preferably in the clinical research industry Good understanding of global clinical trial practices, procedures, methodologies and regulatory Experience with R programming is essential requirements (e.g., GCP, ICH More ❯

Responsible for all statistical programming/data review reporting and analytics development aspects of several studies, a medium to large sized project or project-level activities. Acts as a key collaborator and strategic partner in ensuring that drug-development plans are executed efficiently with timely and high quality deliverables. Complies with project/study standards and specifications following internal … and regulatory guidelines. Oversees programming style, quality of statistical reporting & compliance with timelines. About the Role Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives. To do this, we are optimizing and strengthening our processes and ways of working. We are investing in new technologies and building specific therapeutic area … and help give people with disease and their families a brighter future to look forward to. Apply today and welcome to where we thrive together! The Role The Principal Statistical Programmer is responsible for all statistical programming aspects of a large/pivotal study, several studies or project-level activities (incl. submission activities). The position is More ❯

Principal Statistical Programmer | Leading CRO | Home Based | UK | Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries Renowned for its high-quality deliverables, exceptional customer service, and flexibility in meeting clients’ needs this growing organisation offers a flexible, dynamic, and entrepreneurial culture. With … ongoing growth and exciting career opportunities, it’s the perfect place to advance your career. We’re seeking elite Principal Statistical Programmers to join this growing organisation remotely from anywhere in the UK. What you will be doing: You’ll lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM … compliance with SOPs. What you will need: A Bachelor’s degree in Statistics, Biostatistics or Computer Sciences + Masters or PH.D in Statistics. 8 years’ experience in clinical trial statistical programming. Excellent knowledge of SAS essential with R advantageous. Good working knowledge of data structures e.g. CDISC, SDTM, ADaM, Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines. More ❯

work with many of the most advanced drugs, biologics, and medical devices in development today. Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham … that's Everest. To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Senior Statistical Programmer remotely from a home-based office anywhere in the the UK in accordance with our Work from Home policy. Key Accountabilities Design and specify study data tabulation … the integration of clinical trial data from multiple trials (e.g. ISS and ISE datasets). These designs and specifications are completed in accordance with common industry standards and conventions, statistical requirements and specifications, and/or clinical trial sponsor's requirements. Generate complete and efficient analysis data models following approved dataset designs or specifications. Perform independent validation of datasets More ❯

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. As a growth-oriented medium-sized company with over 145 employees, we operate internationally. Our customers appreciate the competence and commitment of our employees and we value our employees as the basis of … the company's success. Join a motivated and friendly team as Statistical Programmer (UK Remote) Your responsibilities You program and validate statistical analysis of clinical studies with SAS. You define and program analysis datasets and CDISC SDTM and ADaM datasets in SAS. You are responsible for the quality control of evaluations of clinical studies. You conduct all More ❯

Job Description Summary Responsible for all statistical programming, data review, reporting, and analytics development aspects of several studies, including medium to large-sized projects or project-level activities. Acts as a key collaborator and strategic partner to ensure efficient execution of drug development plans with timely and high-quality deliverables. Ensures compliance with project/study standards and specifications … following internal and regulatory guidelines. Oversees programming style, quality of statistical reporting, and adherence to timelines. Job Description Our Development Team is guided by our purpose: to reimagine medicine to improve and extend people's lives. We are optimizing and strengthening our processes and ways of working, investing in new technologies, and building therapeutic area and platform capabilities to … join us and help give people with disease and their families a brighter future. Apply today and join a team where we thrive together! The Role The Senior Principal Programmer is responsible for all statistical programming aspects of several studies or project-level activities, including submission and post-marketing activities. The role is a key collaborator and strategic More ❯

Tech Observer is hiring Senior Statistical Programmers and Principal Programmers in UK and Europe on FSP. Job Responsibilities (But not limited to) Carry out all activities according to Tech Observer SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Ensure adherence to programming guidelines. Implement and follow the latest versions of … CDISC, FDA Guidelines, GCP and other industry standards; Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). Review and interpret Report and Analysis Plans and provide comments for assigned projects. Develop and review SAS programs and output for the management of … clinical trial data, the tabulation of data, preparation of patient data listings, graphical output, and creation of derived datasets and statistical analysis of data as specified in the Statistical or Report Analysis Plans. Develop SAS programs for ad hoc tables and listings. Write, modify, and maintain programs that produce diagnostics and listing for data review in support of More ❯

Start your journey with purpose, passion, and people who care. At Abbott, we believe in more than just careers - we believe in calling. For over 135 years, we've been helping people live fuller, healthier lives. And we know that More ❯