What are the responsibilities and job description for the SAS Viya Developer position at TechClub Inc?
SAS Viya Developer
Locatio
nRaleigh, NC (Hybrid/Onsite
)
Role Overvi
ewWe are seeking a highly experienced SAS Viya devloper with experience between 5 to 10 years of expertise in clinical data programming, CDISC standards, and cloud-based analytics platforms. The ideal candidate will lead end-to-end clinical data workflows, regulatory submissions, and modern data platform transformations in GxP-regulated environment
s.This role requires strong domain expertise in SDTM, ADaM, regulatory submissions, and SAS/Python/R programming, combined with experience in cloud platforms (AWS/Azure) and clinical data modernization initiative
s.______________________________________
__Key Responsibiliti
esClinical Data Programming & Regulatory Submissio
ns• Design, develop, and validate SDTM and ADaM datasets in compliance with CDISC standar
ds• Lead generation of define.xml, aCRF/eCRF annotations, and submission-ready deliverabl
es• Develop and optimize automated submission pipelines for FDA and global regulatory authoriti
es• Ensure compliance with GxP, 21 CFR Part 11, HIPAA, and ICH E6 guidelin
esData Engineering & Automati
on• Architect and implement end-to-end clinical data pipelines using SAS, Python, and
R• Develop reusable SAS macro libraries and automation framewor
ks• Build scalable data pipelines including modern formats (JSON/XPT alternative
s)• Drive migration from legacy systems to modern data architectur
esCloud & Platform Engineeri
ng• Lead implementation and optimization of SAS Viya platforms on AWS/Azu
re• Manage cloud infrastructure components (EKS, EC2, EFS, FSx, Databricks, etc
.)• Implement FinOps practices for cost governance and optimizati
on• Evaluate and onboard next-gen analytics platforms (e.g., Databrick
s)Leadership & Stakeholder Manageme
nt• Lead cross-functional teams across US, UK, and offshore locatio
ns• Collaborate with clinical, statistical, regulatory, and IT stakeholde
rs• Drive Agile delivery and sprint planning for data and platform initiativ
es• Manage vendor relationships, tool selection, and licensing strategi
esCompliance & Governan
ce• Ensure adherence to regulatory and audit requirements (FDA, OCC, SOX, Basel III as applicabl
e)• Maintain audit-ready documentation and validation process
es• Implement data governance, traceability, and reproducibility standar
ds______________________________________
__Required Qualificatio
ns• Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or related fie
ld• 15 years of experience in statistical programming and clinical data manageme
nt• Strong expertise i
n:o SAS (Base, Macro, SQL, ODS, STAT, Grap
h)o CDISC standards (SDTM, ADaM, define.xm
l)o Regulatory submissions (FDA, global agencie
s)• Hands-on experience wit
h:o Python (Pandas) and/or R (admiral, Shin
y)o Cloud platforms (AWS/Azur
e)• Strong understanding of GxP and clinical compliance framewor
ks______________________________________
__Preferred Qualificatio
ns• Experience with SAS Viya architecture and administrati
on• Familiarity with Databricks, DBT, or modern data engineering too
ls• Knowledge of CI/CD tools (Jenkins, Gi
t)• Experience in financial/regulatory environments (Basel III, CCAR, OCC) is a pl
us• AWS or cloud certificatio
ns______________________________________
__Key Skil
ls• Clinical Data Standards: SDTM, ADaM, CDI
SC• Programming: SAS, Python, R, S
QL• Cloud: AWS, Azu
re• Tools: Pinnacle 21, Git, Jenkins, Power BI, Grafa
na• Methodologies: Agile, DevOps, Data Governan