Axiom Path
Be Part of a Dynamic Biostatistics & Biometrics Team
This global biopharmaceutical company is dedicated to advancing therapies for serious and rare diseases. The Biometrics team plays a key role in driving data integrity and analytical excellence across clinical development programs. The group fosters a collaborative and innovation-driven culture where data programming expertise directly contributes to regulatory success and clinical insights.
What’s In Store For You This is a full-time, contract-based opportunity located in Bridgewater, NJ. The role offers exposure to cutting-edge statistical programming initiatives and the chance to collaborate with highly skilled biostatisticians and data scientists supporting high-impact clinical studies.
How You Will Make An Impact
Provide programming support for clinical trials and submission deliverables.
Develop and maintain SDTM and ADaM datasets compliant with CDISC standards.
Produce tables, figures, and listings for clinical studies and publications.
Collaborate cross-functionally with Biometrics and Biostatistics teams.
Build and maintain robust SAS macros and utilities to optimize workflows.
Ensure quality, consistency, and efficiency in all programming deliverables.
Are You an Experienced SAS Programming Professional Ready to Make an Impact?
Bachelor’s degree in Mathematics, Statistics, Computer Science, or related field.
5 years of experience in SAS programming within the pharmaceutical or biotech industry.
Strong expertise in CDISC standards (SDTM and ADaM).
Experience supporting data for regulatory submissions.
Familiarity with additional programming tools such as R, Python, or VBA is an asset.
Strong attention to detail, communication, and organizational skills.
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What’s In Store For You This is a full-time, contract-based opportunity located in Bridgewater, NJ. The role offers exposure to cutting-edge statistical programming initiatives and the chance to collaborate with highly skilled biostatisticians and data scientists supporting high-impact clinical studies.
How You Will Make An Impact
Provide programming support for clinical trials and submission deliverables.
Develop and maintain SDTM and ADaM datasets compliant with CDISC standards.
Produce tables, figures, and listings for clinical studies and publications.
Collaborate cross-functionally with Biometrics and Biostatistics teams.
Build and maintain robust SAS macros and utilities to optimize workflows.
Ensure quality, consistency, and efficiency in all programming deliverables.
Are You an Experienced SAS Programming Professional Ready to Make an Impact?
Bachelor’s degree in Mathematics, Statistics, Computer Science, or related field.
5 years of experience in SAS programming within the pharmaceutical or biotech industry.
Strong expertise in CDISC standards (SDTM and ADaM).
Experience supporting data for regulatory submissions.
Familiarity with additional programming tools such as R, Python, or VBA is an asset.
Strong attention to detail, communication, and organizational skills.
dice #J-18808-Ljbffr