Senior Statistical Programmer - Fsp

Experteer Overview In this role, you will design, develop, and QC SAS programs to access, transform, and submit clinical data in CDISC ADaM format.You will collaborate with study teams to ensure submission-ready data and output for SDTM/ADaM, tables, figures, and listings.You will lead complex SAS programming for pooled and exploratory analyses and help deliver ISS/ISE datasets when needed.You’ll drive efficiency through global tools and work with cross-functional teams to meet timelines.Compensaciones / Beneficios - Design data structures and specifications for ADaM datasets, Tables, Figures, Listings and Analysis Submission content - Ensure submission readiness of clinical data per SDTM/ADaM standards - Lead pooled and exploratory analyses with statistics leads and programming team - Oversee ISS/ISE dataset delivery and output when CRO not providing - Develop complex SAS programs for ADaM data analysis and reporting - Develop and maintain global tools to improve programming group efficiency - Coordinate with study teams to meet timelines and quality deliverables - Collaborate with Ru**D staff on data analysis requests - Support regulatory responses, integrated safety/efficacy summaries, publications, and exploratory analysesResponsabilidades - 5+ years of experience in clinical or statistical programming in CRO/pharma - Strong SAS programming, including macro development - Hands-on R programming experience - Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM) - Proven leadership in programming activities for pooled/exploratory analyses - Ability to work independently and in cross-functional teams - Experience with multi-study submission processes and timelines - Experience with legacy data in clinical trialsRequisitos principales - remote work - home-based role - flexible work arrangement - autonomy and balance - collaborative tools - global team environment

You will lead complex SAS programming for pooled and exploratory analyses and help deliver ISS/ISE datasets when needed. You’ll drive efficiency through global tools and work with cross-functional teams to meet timelines.Compensaciones / Beneficios - Design data structures and specifications for ADaM datasets, Tables, Figures, Listings and Analysis Submission content - Ensure submission readiness of clinical data per SDTM/ADaM standards - Lead pooled and exploratory analyses with statistics leads and programming team - Oversee ISS/ISE dataset delivery and output when CRO not providing - Develop complex SAS programs for ADaM data analysis and reporting - Develop and maintain global tools to improve programming group efficiency - Coordinate with study teams to meet timelines and quality deliverables - Collaborate with Ru**D staff on data analysis requests - Support regulatory responses, integrated safety/efficacy summaries, publications, and exploratory analysesResponsabilidades - 5+ years of experience in clinical or statistical programming in CRO/pharma - Strong SAS programming, including macro development - Hands-on R programming experience - Advanced knowledge of CDISC standards (CDASH, SDTM, ADaM) - Proven leadership in programming activities for pooled/exploratory analyses - Ability to work independently and in cross-functional teams - Experience with multi-study submission processes and timelines - Experience with legacy data in clinical trialsRequisitos principales - remote work - home-based role - flexible work arrangement - autonomy and balance - collaborative tools - global team environment