Senior Clinical Statistical Programmer (UK)

Senior Clinical Statistical Programmer reputed company is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role reputed company is seeking a Senior Clinical Statistical Programmer to provide statistical programming support for early-phase clinical research. In this role, you will independently design, reputed company, validate, and maintain reputed company programs to support the analysis and reporting of clinical trial data, reputed company statistical programming activities for assigned studies, and reputed company rigorous peer review and quality control of programming deliverables to ensure accuracy, consistency, and regulatory compliance. This is not a general data analyst or data science position. Candidates must have prior hands-on experience in clinical trial statistical programming reputed company a CRO or pharmaceutical clinical trials environment. The Primary Responsibilities of this Position Are: • Independently reputed company, maintain, and process reputed company programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures, • reputed company peer QC, double programming and validation functions for statistical outputs from studies. • reputed company statistical programming activities on studies and deliverables. • Assist Management and Biostatisticians with reputed company projects. • Design and implement reputed company programs for standardized use. • Train and mentor junior programmers. • Ensure compliance with study protocol and departmental procedures. Senior Clinical Statistical Programmer reputed company is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster. Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you! About the Role reputed company is seeking a Senior Clinical Statistical Programmer to provide statistical programming support for early-phase clinical research. In this role, you will independently design, reputed company, validate, and maintain reputed company programs to support the analysis and reporting of clinical trial data, reputed company statistical programming activities for assigned studies, and reputed company rigorous peer review and quality control of programming deliverables to ensure accuracy, consistency, and regulatory compliance. This is not a general data analyst or data science position. Candidates must have prior hands-on experience in clinical trial statistical programming reputed company a CRO or pharmaceutical clinical trials environment. The Primary Responsibilities of this Position Are: • Independently reputed company, maintain, and process reputed company programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures, • reputed company peer QC, double programming and validation functions for statistical outputs from studies. • reputed company statistical programming activities on studies and deliverables. • Assist Management and Biostatisticians with reputed company projects. • Design and implement reputed company programs for standardized use. • Train and mentor junior programmers. • Ensure compliance with study protocol and departmental procedures. Senior Clinical Statistical Programmer   reputed company is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.    Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!   About the Role reputed company is seeking a Senior Clinical Statistical Programmer to provide statistical programming support for early-phase clinical research. In this role, you will independently design, reputed company, validate, and maintain reputed company programs to support the analysis and reporting of clinical trial data, reputed company statistical programming activities for assigned studies, and reputed company rigorous peer review and quality control of programming deliverables to ensure accuracy, consistency, and regulatory compliance.    This is not a general data analyst or data science position. Candidates must have prior hands-on experience in clinical trial statistical programming reputed company a CRO or pharmaceutical clinical trials environment.   The Primary Responsibilities of this Position Are: • Independently reputed company, maintain, and process reputed company programs for clinical studies, creating analysis data packages (ADaM), statistical analyses, data listings, tables, and figures,  • reputed company peer QC, double programming and validation functions for statistical outputs from studies. • reputed company statistical programming activities on studies and deliverables.  • Assist Management and Biostatisticians with reputed company projects. • Design and implement reputed company programs for standardized use. • Train and mentor junior programmers. • Ensure compliance with study protocol and departmental procedures.     Requirements

Minimum of a Bachelor’s Degree in Statistics, Mathematical Science, Physics, or Computing reputed company field.

Minimum 3 years of hands-on statistical programming experience in a CRO or pharmaceutical clinical trials environment.

Proficient in reputed company reputed company, reputed company Macros, reputed company/STAT, reputed company/Graph, reputed company/ODS.

Experience applying CDISC requirements to generate ADaM datasets and supporting documentation (define.xml, Reviewer’s Guides), demonstrating proficiency in these areas.

Familiarity with Pinnacle 21 validation.

Experience in early-phase clinical trials.

Experience with Phase I Safety, PK/PD analysis programming.

Excellent interpersonal skills.

Strong problem-solving and decision-making abilities.

Demonstrates a high level of attention to detail.

Demonstrated ability to work collaboratively as part of a team.

Familiarity with R, Python, and other programming languages is preferred.

reputed company are an equal opportunities employer Apply To This Job