Clinical SAS Programmer
Job Description
Katalyst Healthcares & Life Sciences is hiring entry-level candidates for several positions for contract research in Clinical trials of drugs, biologics, and medical devices. We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies, and recruiting partners. Job Description Hands-on statistical programming experience in the pharma/biotech industry. Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros, preferable experience using R. Desire to understand the disease area, protocol, SAP, and study-related documents. Good knowledge of clinical trial design and statistical terminology. Strong knowledge of CDISC SDTM and ADaM data models. Demonstrated proficiency in developing dataset specifications and using SAS/R to produce SDTM datasets, ADaM datasets, and TFLs. Thorough understanding of clinical data structures and data exchange with multiple data formats. Expertise in performing validation of datasets and TFLs using a risk-based approach. Expertise in regulatory submissions and preparation of e-sub package. In-depth understanding of regulatory, industry, and technology standards and requirements. Exceptional organizational, communication, and time management skills, with the ability to multi-task across projects. Demonstrated ability to work in a team environment with cross-functional teams. Qualifications Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat, and SAS Macros, preferable experience using R. Strong knowledge of CDISC SDTM and ADaM data models. Demonstrated proficiency in developing dataset specifications and using SAS/R to produce SDTM datasets, ADaM datasets, and TFLs. Expertise in regulatory submissions. Additional Information All your information will be kept confidential according to EEO guidelines. #J-18808-Ljbffr