Katalyst Healthcares and Life Sciences
Clinical SAS Programmer
Katalyst Healthcares and Life Sciences, Boonton, New Jersey, us, 07005
Responsibilities:
Process, manage, and analyze registry study and large claims databases.Master's degree in health economics and outcomes research, statistics, mathematics, psychology, epidemiology, computer science, or related fields.Provide input into the development of programming environments.Design and implement macro/library codes (e.g., SAS macros).Learn subject matters and new statistical methods.Manage multiple projects to meet timelines.ssist in developing statistical analysis plans and outputs to support internal strategy development and external communications.Demonstrate knowledge of real-world evidence (RWE) databases and clinical trial data.pply various statistical methods to real-world research and clinical trial studies.Requirements:
Strong and advanced programming and analytical abilities in SAS/SQL/R/Python.Experience in data processing, statistical methods application, and results interpretation.Demonstrated experience in observational research and study design.Project management skills.Good written and oral communication skills in English.Minimum years of programming experience in SAS/SQL/R/Python, with at least 3-5 years in the pharmaceutical industry.
Process, manage, and analyze registry study and large claims databases.Master's degree in health economics and outcomes research, statistics, mathematics, psychology, epidemiology, computer science, or related fields.Provide input into the development of programming environments.Design and implement macro/library codes (e.g., SAS macros).Learn subject matters and new statistical methods.Manage multiple projects to meet timelines.ssist in developing statistical analysis plans and outputs to support internal strategy development and external communications.Demonstrate knowledge of real-world evidence (RWE) databases and clinical trial data.pply various statistical methods to real-world research and clinical trial studies.Requirements:
Strong and advanced programming and analytical abilities in SAS/SQL/R/Python.Experience in data processing, statistical methods application, and results interpretation.Demonstrated experience in observational research and study design.Project management skills.Good written and oral communication skills in English.Minimum years of programming experience in SAS/SQL/R/Python, with at least 3-5 years in the pharmaceutical industry.