Sr Programmer Analyst II
Role Overview
The Senior Programmer Analyst performs advanced bioinformatics programming activities for research projects.
The role supports statistical and computational requirements for clinical studies.
The position independently leads selected moderately complex studies and may support more complex studies under a lead programmer.
Key Skills for This Role
Full Job Posting
Work Schedule
- The standard work schedule is Monday through Friday.
Role Overview
The Senior Programmer Analyst performs advanced bioinformatics programming activities for research projects.
The role supports statistical and computational requirements for clinical studies.
The position independently leads selected moderately complex studies and may support more complex studies under a lead programmer.
Programming and Bioinformatics
- Create, execute, maintain, and validate programs that transfer, combine, summarize, and report data.
- Validate SAS programs that generate listings, tables, and figures.
- Work with multiple data management systems, operating systems, data sources, and database structures.
Study Leadership and Quality
- Lead programming for selected studies of moderate complexity.
- Work with project leaders, client representatives, and multidisciplinary clinical trial teams.
- Assess project goals and timelines and manage assignments to meet delivery requirements.
- Provide quality control review for statistical programming.
Training and Departmental Support
- Train and mentor junior team members and contribute to professional development.
- Support training materials, departmental documents, policies, working practice documents, and SOPs.
- Represent the company at conferences and present or teach at department meetings.
- Support the bidding process as requested.
Education and Experience
- A bachelor's or master's degree in computer science, statistics, biostatistics, mathematics, or a related field, or an equivalent qualification, is required.
- At least 6 years of relevant statistical programming, clinical programming, or related experience is required.
- Clinical trial experience in the pharmaceutical, biotechnology, or CRO industry is required.
- Strong SAS programming experience is required.
Knowledge and Skills
- Knowledge of programming languages, relational databases, and complex data systems.
- Strong problem-solving, communication, organizational, leadership, and collaboration skills.
- Proficiency in English and ability to manage multiple assignments under challenging timelines.
- Ability to capture biostatistical metrics and provide statistical programming quality control.
Working Environment
- Work is performed in an office environment with exposure to electrical office equipment.
- Occasional domestic and international travel to site locations may be required.
About Thermo Fisher Scientific
Thermo Fisher Scientific promotes scientific innovation, collaboration, professional development, and scientific excellence.
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