Senior Statistical Programmer Consultant

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UKContractSenior

Salary not disclosed

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Job Details

Experience: 5 years with Bachelor's degree or 6 years with Master's degree in clinical programming (CDISC)

Requirements

Strong SAS programming experience within the pharmaceutical/CRO industry
Hands-on experience supporting CVRM (Cardiovascular, Renal & Metabolism) studies
Experience in generating and validating SDTM, ADaM, and TLFs
Good understanding of CDISC standards and clinical trial processes
Respiratory/Immunology therapeutic area (TA) experience
Working knowledge of ICH and Good Clinical Practices
Strong communication and stakeholder management skills
Bachelor's or Master's degree in computer science, statistics, or related scientific discipline
Experience supporting regulatory submissions is preferred

Responsibilities

Lead and support programming efforts for clinical study components
Develop, validate, and maintain SAS programs for analysis and reporting
Create datasets, tables, listings, and figures
Collaborate with Biostatistics, Data Management, and Clinical teams
Ensure deliverables meet quality standards and timelines
Participate in study planning and review specifications
Support regulatory submission activities

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