Job details

Biostatistical SAS Programmer

Bachelors or Master’s degree in relevant fields.
8+ years of relevant professional experience in a leadership position creating SDTM & ADaM deliverables.
Understands how clinical studies are run and managed and submitted to regulatory agencies across the globe and has worked as a TA or compound lead for at least 5+ studies over 2+ organizations over the last 5 years
Has significantly improved efficiency in Clinical Trials by digitizing processes, consolidating processes, or introducing extreme automation for manual processes
Will be responsible for defining next generation solution that helps in Clinical trial effectiveness and submission pathway.

Strong experience with developing submission outputs – e.g. SDTM datasets, ADaM datasets, define.XML, TLG (table listing and graphs)
Hands on experience developing programs to create SDTM & ADaM outputs (multiple studies)
Ability to provide specifications for automating creation of SDTM & ADaM outputs
Deep expertise with EDC & other clinical data sources (e.g. Lab)
Deep experience in all the Biostats process (patient data analytics, cross trial analytics)
Ability to create visualizations on SDTM & ADaM data
Experience in performing the business process SDTM & ADaM conversion
Should be leading a team performing the Biostats activities (preferably from Pharma or CRO)
Apart from SAS, Programming experience in another language e.g. R,python) will be a plus

Founded in 1997, Saama Technologies is an advanced clinical data and analytics company. Saama’s AI-driven clinical data analytics platform integrates, curates, and animates sources of structured, unstructured, and real-world data to deliver insigh...

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DEPARTMENTS

Research & Development

SENIORITY LEVEL REQUIREMENT

Senior

INDUSTRY

Information Technology

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