Sr Programmer Analyst II

Work Schedule

• Standard Monday through Friday schedule.

Work Environment

• Work is performed in an office environment.
• The role includes occasional travel to site locations and occasional domestic and international travel.

Role Overview

Programming and Bioinformatics

• Create, execute, maintain, and validate programs that transfer, combine, summarize, and report data across multiple systems and sources.
• Validate SAS programs that generate listings, tables, and figures.

Study Leadership and Project Management

• Lead selected moderately complex studies and work with project leaders, client representatives, and multidisciplinary clinical-trial teams.
• Assess project goals and timelines and communicate actively with team members.

Quality and Development

• Manage and document assignments, maintain awareness of contractual obligations, and provide quality control review for statistical programming.
• Train and mentor junior team members and develop professional skills in programming, clinical trials, and the pharmaceutical industry.

Departmental Support

• Support conferences, department presentations, training materials, departmental documents, policies, working-practice documents, SOPs, and bidding activities.

Required Qualifications

• Bachelor’s or Master’s degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, or an equivalent relevant qualification.
• Minimum 6 years of relevant experience in statistical or clinical programming or a related field.
• Experience supporting clinical trials in the pharmaceutical, biotechnology, or CRO industry.
• Strong SAS programming experience.

Knowledge and Skills

• Knowledge of programming languages, relational database structures, and complex data systems.
• Strong problem-solving, communication, collaboration, organization, adaptability, leadership, and mentoring abilities.
• Proficiency in English and ability to provide quality control review for statistical programming.