Duration
6-12+ Months – 20 hours for the first Month THEN Ad-hoc work after, 8-15 hours per MONTH
Job Description
- First 20 hours in Month 1: Client has a few studies that need to be verified, need to do a interim analysis on the studies with assessment on the statistical power. Then will be working with the team to determine the best methodology to design the study with the ultimate goal of publishing a paper.
- Defining an achievable statistical standpoint.
- This consultant will work on a part-time / Ad HOC basis on reviewing a few dozen active studies, they will receive a large database and they merge test results with patient info clinical risk factors and outcomes and then analyzing that data. The consultant can make suggestions on how to analyze the data. Test results vs outcome. Prereq to show multivariable analysis the biomarker is actual and how do they combined it to other variables like PSA, prostate exams, family history, etc. There will be modeling, Hazard ratios, odds ratios and scrubbing raw data while working with the clinical team.
Required Skills
- Oncology, Clinical Utility, SAS license or know how to program in R to make the scripts
Plus/Nice to have
- Prostate Cancer, GU Cancer, PhD in Biostats (experience outweighs degree), involvement with peer review publication, Molecular Diagnostics
Remote: Oncology Diagnostics Biostatical SME (235108)
#LI-Remote
