5 of 5 Permanent CDISC Jobs in Berkshire

visualization tools. Proven ability to manage multiple projects and coordinate with external vendors. Mastery of SAS programming for clinical trial data analysis. Knowledge of CDISC standards and regulatory submission requirements. Strong problem-solving skills with a focus on automation and process improvement. Ability to adapt to a fast-paced, dynamic More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

reporting tasks. Expert Level (6+ years): Deep expertise in data analytics and clinical reporting. Proven ability to lead projects and mentor teams. Familiarity with CDISC standards and advanced reporting infrastructure. Desired Competencies Strong analytical and problem-solving skills Excellent communication and stakeholder management Experience working in a matrixed, cross-functional More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … 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. What in it for you: The opportunity to be involved in a growing More ❯

lead statistical programming projects, ensuring high-quality, on-time deliverables. This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance. You’ll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions. You'll also create define.xml files, develop and … 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. What in it for you: The opportunity to be involved in a growing More ❯