Statistical Programmer I / II

• You'll support statistical programming activities across clinical trials, ensuring high-quality and timely deliverables.
• This includes developing and validating SDTM and ADaM datasets, performing QC checks, and ensuring CDISC compliance.
• You'll assist with resolving Pinnacle 21 validation issues, contribute to the production and review of TLFs, and support regulatory submission activities. You will also help create define.xml files, develop and maintain SAS programs and macros, perform data integrity checks, and ensure appropriate documentation in line with SOPs., Data Scientist Placement Programme - No Experience RequiredOur training will help you kick-start a new career as a Data Scientist.We are recruiting for companies who are looking to employ our Data Science Traineeship graduates to keep up with their growth. The best part is..., Job Title: Director Study Management (Director Statistics) Duration of Contract: 12 Months IR35 Status: Outside About the Role AZ are seeking an experienced and visionary Statistics Director to join our Team and lead strategic statistical innovation across AZ's...

• A Master's or Ph.D. degree in Statistics, Biostatistics, Computer Science, or a related field.
• Approximately 3-5 years of experience in clinical trial statistical programming.
• Excellent knowledge of SAS is essential, with R considered advantageous.
• Good working knowledge of clinical data standards such as CDISC, SDTM, and ADaM.
• Understanding of TLFs, clinical data structures, and regulatory submission requirements.

• The opportunity to be involved in a growing organisation.
• Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
• Fully remote role within the UK.
• Competitive remuneration package.

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