Programmer Analyst II

Role overview

Responsibilities

• Create, run, maintain, and validate programs for data transfers, data integration, summaries, reports, listings, tables, and figures.
• Prepare and analyze clinical trial datasets covering laboratory, vital signs, tumor response, imaging, quality of life, and adverse events.
• Collaborate with researchers and project teams to understand needs, analyze problems, and recommend technology-based solutions.
• Develop customized code to produce or validate clinical bioinformatics and technical outputs.
• Lead programming tasks on simple to moderately complex studies and, under close supervision, lead projects as appropriate.
• Follow departmental procedures and contribute to training materials and departmental documents and policies.

Education and experience

• Master’s degree in computer science, statistics, biostatistics, mathematics, or a related field; alternatively, a bachelor’s or equivalent degree with relevant formal academic or vocational qualifications.
• At least four years of end-to-end SDTM experience, including programming and delivery of SDTM datasets.
• Relevant experience demonstrating the knowledge, skills, and abilities required for the role.

Knowledge and skills

• Solid understanding of one or more programming languages and relational database structures and complex data systems.
• Good attention to detail and problem-solving skills; clear written and verbal communication and proficiency in English.
• Ability to manage multiple assignments and challenging timelines, collaborate, take initiative, and adapt to changing priorities.

Working conditions

• Work is performed in an office environment with exposure to electrical office equipment.
• Occasional driving to site locations and occasional domestic or international travel may be required.
• Standard Monday-to-Friday work schedule.