We are seeking an experienced Biostatistics consultant for an initial 12-month contract with strong opportunity for extension. They will be responsible for applying relevant statistical methods to clinical trial data analysis for crucial Phase II and III studies.
Responsibilities:
-Phase II and III trial readout and ad hoc analysis and reporting
-Review the Biostatistics and Statistical Programming Analysis (SPA) generated statistical TLFs and supporting the preparation of regulatory documents
-Provide ad-hoc data listings and summary information per requests
-Perform quality control
The Ideal Candidate:
-Ph.D. degree or equivalent education in Biostatistics with a minimum of 5 years relevant experience in biotech/pharma inustry
-Experience with oncology trials preferred
-Demonstrated proficiency with SAS
-Experience managing external vendors and CROs
-Ability to work cross-functionally
-Excellent communication skills
