Programmer Analyst II

Make an Impact at the Forefront of Innovation. The Programmer Analyst II performs bioinformatics programming activities for the statistical and computational considerations of research projects. Additionally, the Programmer Analyst serves on a study team under the direction of a Lead Programmer. Perform programming tasks as assigned by study/project team leads, including but not limited to independently creating, executing, maintaining, and validating programs that transfer data across multiple data management systems or operating systems; combining data from a variety of sources and structures; generating and storing summary data from a variety of sources; generating reports or combining multiple databases; and validating programs that generate listings, tables, and figures using SAS and standard tools and processes. Prepare and analyze clinical trial patient datasets such as laboratory data, vital signs data, tumor response data, imaging data, quality-of-life and well-being questionnaire data, or adverse events data for clinical research purposes. Develop customized code to utilize existing tools and applications to provide outputs or validate outputs for clinical, bioinformatics, or technical use. Function as a contributing member of a multidisciplinary team and, under the oversight and review of management, may begin to assist with some lead programming activities. Increase knowledge base and professional skills in areas including programming technology and techniques, clinical trials, and the pharmaceutical industry by working closely with mentors, attending presentations and teaching events, and contributing to other general department documents and policies by assisting mentors with implementing best practice documents and articles. MS/MA degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field and abilities to perform the job; or a Bachelor’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, or equivalent and relevant formal academic/vocational qualification. Must have at least 4 years of hands-on, end-to-end SAS programming experience in clinical trials, including strong experience with SDTM, ADaM, and TLF programming. Satisfactory problem-solving skills. Satisfactory written and verbal communication skills. Solid understanding of relational database structures and complex data systems. Occasional drives to site locations with occasional travel, both domestic and international. Job Description. What You’ll Do. Consult with researchers and multidisciplinary project teams to analyze problems and recommend technology-based solutions and computational strategies for the specific project as assigned. Ensure adherence to departmental working practice documents and SOPs and contribute to informal training materials. Education & Experience Requirements. Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Solid understanding of one or more programming languages. Good attention to detail. Proficiency in the English language. Capable of effectively organizing and managing multiple assignments with challenging timelines. Positive attitude and capable of working well with others. Demonstrated initiative and motivation. Good organizational skills and capable of adapting and adjusting to changing priorities. Work is performed in an office environment with exposure to electrical office equipment.