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Freelance Biostatistician / Senior Programmer - Belgium
I am currently working on behalf of a European CRO in the search for a Biostatistician / Senior Programmer to join their team based in the Belgium.
My client are looking for an experienced individual who has been involved with SAS stat and SAS Graph within a clinical setting, analysing data produced within a variety of clinical trials. You will work closely with cross functional teams in support of the development of regulatory documentation across the clinical trial.
Drives the interpretation of results and the development of key messages to the wider development team
Deliver statistical consultation for interpretation requests and design of methodologies to support analysis.
Follow client protocols and procedures and be responsible for high quality of deliverables
Author and review protocols, stats analysis plans DPP, CRF and CRS documents.
Support the clinical and regulatory teams with timely informatics.
The successful candidate will be a highly motivated individual who is able to work within a commercially aware team that are working to tight timelines and have the ability to support the organisation in successful trial delivery and continue to deliver multiple exemplary standard proposal documents concurrently will be essential.
The role will be working on client site in Belgium for the first six months with some flexibility to be home based after for a couple of days a week.
For the detailed information and rate confirmation please send your up to date CV to Richard.email@example.com
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