Biostatistician

BIOSTATISTICIAN

3 - 6mth initial contract (potential extension)

Hybrid IDEALLY, if not MUST be in PST

• Apply knowledge of basic and complex statistical design, analysis, and programming techniques utilized in clinical research.
• Develop and reviews statistical analysis plans based on study-specific documents and sound statistical methodology.
• Develop, maintain, and produces statistical programs and specifications used in creating analysis datasets, tables, listings, and figures.
• Coordinate with programmers and data management personnel as to database maintenance, updating, and documentation. Provide guidance for database structures for analysis.
• Programs/validate statistical tables with an emphasis on efficacy endpoints. Provide proper documentation and oversees the work of others who assist in programming/validating.
• Understand and comply with all company policies and standard operating procedures.
• Maintain a professional working relationship with sponsors, collaborating associates, and vendor personnel.

Requirements:

• Ph.D. with 3+yrs experience, or a Master's degree with 5+ yrs experience in Biostatistics, Statistics, or a similar field.
• Must have Sponsor experience, not solely CRO or academic.
• Experience within Diabetes is required
• Lead Experience.
• Comfort with data read outs and strategy following.
• Knowledge of FDA and ICH Guidelines required.
• Knowledge of statistical design, analysis, and programming techniques utilized in clinical research required.
• Good SAS® programming skills and understanding of database structures
• Ability to work on multiple projects at once
• Sense of ownership and pride in your performance and its impact on the company's success
• Good time-management skills
• Excellent interpersonal, written, and oral communication skills.