Responsibilities :You will provide technical expertise as an experienced R programmer to develop process methodology, ensuring the department meets the needs of both internal and external clients.Responsibilities include planning and coordinating the development of integrated programming solutions across a broad range of statistical programming requirements.You will also provide technical leadership and internal consulting services, providing. specifications and conducting user needs analysis for complex projects or specific client requirements.Expertise in R programming and SAS Base, with good knowledge of SAS Graph and SAS Macros.Ability to implement advanced statistical procedures based on biostatistician specifications.Excellent application development skills with extensive experience in clinical trial data manipulation, analysis, and reporting.Strong knowledge of relational database components and theory.Perform all responsibilities associated with the Senior Programmer role.Assist Senior Programmers and Programmers in their daily activities.Act as the escalation point for Senior Programmers and Programmers.Regularly communicate with sponsors regarding the programming aspects of the project, anticipating issues proactively and collaborating on resolutions.Provide input and/or write programming specifications.Serve as a subject matter expert on all aspects of SAS and R programming.Develop consistent practices for clinical and statistical review of outputs, mentoring programming staff.Ensure consistency across therapeutic areas and oversee the implementation of process improvement initiatives.Maintain expertise with SAS Macros & R and prioritize macro development.Requirements: Bachelor's degree required, preferably in science or mathematics-related fields.Minimum of 5 years of experience in statistical programming in the pharmaceutical or medical device industries.Experience as a technical team lead, directly engaging clients and coordinating tasks within a programming team.In-depth knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and ICH guidelines.Advanced knowledge of R programming, SAS/BASE, SAS/MACRO, SAS/STAT, SAS/GRAPH, SAS/ACCESS, SAS/ODS, SAS/SQL.Familiarity with SDTM and ADaM implementation in accordance with CDISC standards.Strong organizational, interpersonal, leadership, and communication skills.Ability to independently manage tasks and projects while delegating work to team members.Excellent attention to detail and problem-solving abilities.
