Company:
SciPro
Location: South San Francisco
Closing Date: 29/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
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.
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