Seeking a Clinical Statistics Analyst to collaborate with global pharma company's Statistics team in developing data analysis plans, analyzing clinical trial data, and communicating results.
As a Clinical Statistics Analyst, you will work closely with statistical colleagues, physicians, and clinical research scientists to provide input to statistical analysis plans, select statistical methods, and conduct data analysis.
Responsibilities:
- Collaborate with statistical colleagues and study personnel to provide input to statistical analysis plans
- Select statistical methods for data analysis and author corresponding sections of data analysis plan
- Create reporting database and conduct analysis
- Collaborate with data sciences in planning and implementation of data quality assurance plans
- Justify methods selected and implement previously outlined analysis plans
- Conduct peer-review of work products from statistical colleagues
- Maintain proficiency with statistical programming and statistical methodology
- Apply new and varied methods
- Maintain current knowledge of CDISC data standards
- Utilize current technologies and available tools for conducting clinical trial analysis
Requirements:
- M.S., Ph.D., or equivalent experience
- Statistics, Biostatistics, Computer Science
- 5+ years of relevant experience, including 3 major pharma
- Experience in all major phases of drug development
- Regulatory response experience
- High level of expertise in programming
- Proficiency in statistical programming language(s)
- Interpersonal/teamwork skills
- Technical growth and application
- Self-management skills
- Creativity and innovation
- Demonstrated problem solving ability
- Attention to detail
- Data analysis, technology, and systems expertise