Not registered? Sign up for free now.
Planning and performance of statistical analyses for phase I-IV clinical trials and observational studies
Management of projects and project teams
Statistical SAS programming
Creation of relevant documents (e.g. SAPs, TFLs, …)
Preparing and writing of clinical documents (incl. CSPs, CSRs, ICFs, IBs and IMPDs) and medical communication materials
Planning, preparation, compilation and writing of PV documents for regulatory submission in the clinical development, market...
Get jobs on a daily basis for free