Job Overview
Contribute to clinical development of plan preparation;
Review of study protocol and preparation of statistical methodologies;
Programming of study analysis, review of study results and preparation of statistical methods section for clinical / statistical reports;
Communicate project requirements for CRF design, database design and database cleanup to ensure the key study variables are suitable for analysis;
Communicate statistical results to medical writing personnel to ensure accurate interpretation.
Key Requirements
Ph.D. degree in Biostatistics / Statistics with strong experience in SAS Programming or equivalent;
1-2 years of experience in a pharmaceutical or CRO setting preferred.
Fluency in both English
Good knowledge of the Pack Office
Excellent communication skills
FTE: 1.0
Tagged as: biostatistician jobs
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