Biostatistician
We seek a professional with an objective disposition in their approach to the analyses of data. The ideal candidate enjoys getting their hands messy with data.
What you’ll do
- Perform duties of a Study Statistician to support clinical trials of all phases.
- Review work by programmers and programming plans.
- Experience with ADaM data sets is required.
- Contribute to clinical study reports and related activities.
- Prepare statistical analysis plans, specifications for analysis datasets, and table shells.
- Program in SAS (or R) to conduct analyses and to create presentation ready TLFs.
- Review and consult on CRF design and database edit checks.
- Communicate study level resource/quality issues that may impact deliverables or timelines.
- Participate in process improvement initiatives and the development of SOPs.
What we’re looking for
- You are dedicated to continual learning.
- PhD in statistics/biostatistics with 3+ years of clinical trials experience (or MS with 5+ years).
- It’s attractive to be able to conduct simulation studies to evaluate operating characteristics of a statistical method (e.g., adaptive designs, interim analyses, Bayesian methods).
- At the core, you’re humble in your role as a teacher and a consultant to the study team.
- Able to work to strict timelines, including the possibility of urgent deliverables.
Please inquire for the $rate/hour. The position is remote, East Coast time-zone is a plus. Duration is 1-year contract with option to extend or FTE.