senior statistical programmer jobs in United Kingdom

Overview Join to apply for the Senior Statistical Programmer role at TieTalent. A global pharmaceutical company is currently looking for a Senior Statistical Programmer to join their team on a 12-month temporary contract. Why you should apply - Ideal opportunity for a high calibre Statistical Programmer to join a top-20 global pharmaceutical giant. - Fully remote working (with occasional...

Job Description Summary Office Location: London (The Westworks), United Kingdom #LI-Hybrid Hybrid (12 days per month on-site if living within 50 miles of our London office) #LI-Remote Remote (if living beyond 50 miles of our London office) The Early Development, Associate Director, Statistical Programming, is responsible for all statistical programming aspects of one or more drug development...

You will actively engage in team collaborations to meet research goals and report your research findings both internally and externally. You'll use your research to contribute to product development and customer research projects as well as contributing to the company's open source libraries.

You will actively engage in team collaborations to meet research goals and report your research findings both internally and externally. You'll use your research to contribute to product development and customer research projects as well as contributing to the company's open source libraries.

You will be at the forefront of innovation, driving advanced statistical methodologies and translating insights into actionable strategies that influence global health outcomes. If you have a passion for innovation, deep expertise in statistics, and a desire to make a meaningful impact, we invite you to apply for this exciting opportunity.

Overview Office Location: London (The Westworks), United Kingdom. Hybrid (12 days per month on-site if living within 50 miles of our London office). Remote (if living beyond 50 miles of our London office). The Early Development, Associate Director, Statistical Programming, is responsible for all statistical programming aspects of one or more drug development programs or indication programs with...

You will work closely with our Statistics team on projects that involve conducting and presenting the detailed analysis of clinical and health data

You will therefore be exposed to a wide variety of the services offered by Costello Medical and a broad range of therapeutic areas.

Contract Senior / Principal Statistical Programmer – UK (Remote) 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...

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 and quality control process for SAS programs used to access, extract, transform, review, analyze and submit clinical data for all requested...

Senior Statistical Programmer ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. ICON plc is a global leader in healthcare intelligence and clinical research. From molecule to medicine, we...

Tools & Standards Senior Specialist/Statistical Programmer with R (FSP) United Kingdom and 6 more Be the First to Apply Job Description Sponsor-dedicated: Working fully embedded within a tools and standards development team of one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Tools and Standards Specialist you...

When our values align, there's no limit to what we can achieve. Parexel is currently seeking a Senior Statistical Programmer to join us in the UK, dedicated to a single sponsor. Picture Yourself At Parexel: The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support...

You will actively engage in team collaborations to meet research goals and report your research findings both internally and externally. You'll use your research to contribute to product development and customer research projects as well as contributing to the company's open source libraries.

A leading biopharmaceutical company based in the UK is seeking a Principal Statistical Programmer to play a key role in their clinical development programs. The successful candidate will have over 7 years of experience in the Pharma industry, demonstrating exceptional skills in SAS programming and a comprehensive understanding of regulatory submissions. This role requires independent working,...

Why IQVIA This role will be dedicated to one of IQVIA's largest clients through a Functional Service Provider (FSP) type partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you a unique...

You will contribute to the advancement of our clinical studies by developing and validating complex statistical programs, collaborating closely with biostatisticians, and adhering to regulatory standards. What You Will Be Doing: - Designing, developing, and validating SAS programs for statistical analysis and reporting of clinical trial data.

Principal or Senior Statistical Programmer – Remote, Office or Hybrid – UK Permanent position offering home and/or office work, training and support, and a competitive package. Overview Veramed provides high‐standard data management, biostatistics and programming services to clinical trials. The Principal or Senior Statistical Programmer will provide programming support across a range of...

A leading global clinical research organization is seeking a Senior Statistical Programmer in Livingston, United Kingdom. In this role, you will review datasets and provide expertise in SAS program development for analyzing clinical data. The ideal candidate will have over 5 years of experience within a pharmaceutical environment, with strong SAS programming skills and an understanding of CDISC...

You will be responsible for preparing datasets for submission, ensuring compliance with regulatory standards, and collaborating with cross-functional teams in a dynamic environment. Candidates should possess a BSc in Computer Science or related field, with at least 5 years of experience in statistical programming using SAS.

You will be responsible for the design, development, and quality control of SAS programs used for clinical data analysis. Ideal candidates have a BSc in relevant fields and at least 5 years of statistical programming experience, particularly in a CRO/pharmaceutical environment.