Sr. Principal Clinical Trial Statistician

Are you tired of big pharma? At a small pharma company, you can make a bigger impact. Your input will be valued and recognized by all members of the company, including executives at the highest level. We are a growing company, and your skill set will grow as our company grows. Gain experience in the trenches cleaning data with data management, in your code exploring data with innovative advanced statistical methods, and in meetings presenting your findings to leadership.

Responsibilities:

This position will report to the Director of Biostatistics, will be the lead statistician for at least 1 indication and will provide programming support across indications for the Centralized Statistical Monitoring effort. He/she will be responsible for developing automated analyses and visualizations in R and Tableau to facilitate the evaluation of data quality and review at the individual clinical study level as well as accumulating data across multiple clinical studies.

Essential duties include :

1. Directs and leads the statistical input for at least one disease indication
2. Oversees the statistical design, analysis and interpretation of Phase 1-4 clinical trials
3. Actively contributes to global project and study teams as a core member
4. Partners with Data Management and Clinical Monitoring to ensure high quality data deliverables
5. Oversees and reviews deliverables from CROs for the full reporting of clinical trials

Qualifications:

• Bachelor's Degree, Master's Degree or higher in statistics, biostatistics, data science or computer science
• Advanced R or Python programming skills, preferably including ggplot, tidyverse and R Markdown
• Minimum 4 years of experience in data analysis of clinical trials

Skills/Competencies:

• Ability to clearly communicate complex issues, observations and resolutions to management
• Understanding of statistical concepts related to the design and conduct of clinical trials
• Broad experience in data collection, monitoring, cleaning and analysis throughout clinical development (Phase 1-4) preferred
• Previous employment at a pharmaceutical or biotech company or CRO preferred
• Experience explaining results of analyses to non-technical audiences.
• Working knowledge of MS Office suite. Able to generate business correspondence, create forms and generate reports as required
• Have excellent time management skills and are action-oriented, goal-oriented and innovative.
• Experience leading data review discussions and meetings preferred