Job Summary:
We are hiring a Senior Statistical Programmer with expertise in SAS programming and clinical data analysis to support statistical reporting and regulatory submissions. The ideal candidate will independently handle the creation of analysis datasets, statistical reports, and CDISC-compliant deliverables such as SDTM and ADaM, ensuring high-quality output for global clinical trials and regulatory filings.
Key Responsibilities:
Independently perform SAS programming and analysis for clinical datasets, tables, listings, and figures.
Develop and validate SAS application codes.
Handle SDTM and ADaM dataset mapping and generate related deliverables.
Produce outputs required for Clinical Trial Reports (CTR), Integrated Summary of Safety (ISS), and Integrated Summary of Efficacy (ISE).
Support the preparation of safety updates, publications, and meeting presentations.
Collaborate closely with cross-functional teams including clients and internal data management teams.
Act as an expert in one or more programming areas such as SDTM, ADaM, define.xml, statistical graphics, or PK/PD analysis.
Required Skills & Qualifications:
Minimum 10 years of experience in pharmaceutical or CRO industry statistical programming.
Strong expertise in SAS/Base, SAS/Macro, SAS/STAT programming.
Proficiency in CDISC standards, SDTM, and ADaM dataset creation and mapping.
Comprehensive knowledge of statistical programming deliverables for regulatory submissions.
Desirable experience with multiple platforms like Windows and UNIX.
Background in statistics or statistical analysis preferred.
Ability to manage multiple priorities and work independently with minimal supervision.
Perks & Benefits:
Competitive salary package (not specified).
Opportunity to work on global clinical trial data and regulatory submissions.
Professional development and training opportunities.
Collaborative and growth-oriented work environment.
Exposure to leading clinical research tools and data standards.
Company Description:
A reputed global pharmaceutical services provider specializing in biostatistics, clinical programming, and regulatory submissions. The company delivers top-tier solutions to ensure data integrity and regulatory compliance across the pharmaceutical and healthcare industries.
Work Mode:
Remote / Hybrid / On-site (Location Not Specified)
Call to Action:
If you are a skilled SAS programmer ready to drive clinical data excellence, apply now to become part of a global leader in statistical programming and clinical research..
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