SAS Programmer

• Detect errors in detail, corrects them (e.g., review tables/listings, edit checks output and SAS programs to ensure the quality of deliverable), and report it to appropriate personnel (internal or external clients)
• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and the Statistical Programming department.
• Perform and plan the development, implementation, and validation of new process technologies, macros, and applications.
• Fulfill project responsibilities at the level of technical team lead for single studies, under supervision.
• Understand timelines for and milestones affecting their work and alert supervisor to potential slippage.
• Provide training and mentoring to team members All responsibilities are essential job functions unless noted as nonessential.

REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES

• Knowledge of statistics, programming, and/or clinical drug development process.
• In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Ability to implement programming specifications, as appropriate.
• Ability to estimate the programming scope of work and assist in communicating project status.
• Working knowledge of Base SAS, SAS/STAT, SAS Graph, and SAS Macro Language.
• Exhibits routine and occasionally complex problem-solving skills.
• Recognizes when negotiating skills are needed and seeks assistance.
• Good organizational, interpersonal, leadership, and communication skills.
• Ability to effectively handle multiple tasks and projects, under supervision.
• Excellent accuracy and attention to detail
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.