01Responsibilities
Ability to pick up multiple tools/technologies on the job.
Import and Export raw data
Contribute to Mapping specifications
Utilize SAS/R programming/Python programming skills for clinical trial study submissions
Develop programs identifying data issues and reporting them to the appropriate team
Utilize appropriate guidelines to build CDISC/regulatory compliant datasets
Understand CRF annotations and check for consistency with raw data
Ability to debug custom functions/SAS Macros and fix issues
Good understanding of clinical data and domain
Follow Client Processes and SOPs
Assist senior team members in quality control processes
Assist senior team members with team metrics
Communicate with an internal team to create deliverables for pharmaceutical and CRO clients
Work in tandem with Biostatistics and Data Management members on clinical projects
Communicate with programming and statistics leads
Make sure you are compliant with company policies/SOPs.
About US: Saama automates key clinical development and commercialization processes, with artificial intelligence (AI), Generative AI and advanced-analytics, accelerating your time to market. We offer AI-backed SaaS solutions as well as product-based industry services and accelerators. Discover . .
