Description
Our client, a leading pharmaceutical company, is currently seeking an experienced clinical trial statistician for a 6 month contract.
You should have a minimum of a BSc Honours degree in Mathematics/Statistics with experience working in pharmaceutical industry, contract research organization or research institute, and familiarity with advanced statistics methodologies including general linear models, mixed models, survival analysis and categorical data analysis. You should be experienced in all statistical aspects of clinical trials including performing sample size, developing protocols, writing statistical analysis plans, analysing data and writing reports. You should be familiar with SAS and demonstrate an ability to communicate statistical issues to non-statisticians. Ideally you will have experience working with colleagues in global markets, specifically Asia and USA.
In this role you will:
* Provide scientific statistical support & advice.
* Represents department on project teams, coordinates project related activities and develops plans and timelines for the statistical activity on delegated projects.
* Works closely with Clinical, Medical, Statistics and Data Management team members.
* Provide scientific statistical input to development plans and to project planning as needed.
* Provide study design recommendations and prepare sample size calculations for Outline Protocols.
* Prepare statistical section for Clinical Study Protocols. Generate randomisation schedules for clinical trials in accordance with protocols and maintaining security of schedules before and during the studies.
* Review Clinical Protocols. Provide input to the design of Case Report Forms and review discrepancy/edit check specifications.
* Approve Case Report Forms
If you are interested in this role, please forward your CV today.