We are curently seeking 3x Senior or Principal level statistical programmers as part of a significant expansion project for a biometric focused CRO based in the UK.
Our client is looking to double in size by the end of the year due to several new partnerships and projects they have in their pipeline. Very exciting time to be part of a small, fast growing business with long-term stability and excellent development opportunity as they continue to expand.
This position is remote based in the UK only.
Responsibilities:
* Lead statistical programming projects by coordinating study teams, managing timelines, assigning tasks, and ensuring high-quality deliverables while liaising with clients.
* Develop and validate statistical analyses for clinical studies using SAS.
* Create and program analysis datasets, including CDISC SDTM and ADaM standards.
* Perform quality control checks to ensure the accuracy and reliability of study results.
* Support a range of programming tasks required throughout the lifecycle of a clinical study.
Experience required:
* Life Science degree
* Significant experience as a SAS/Statistical Programmer within a CRO or Pharmaceutical environment
* Vast experience programming within SAS
* Significant experience leading studies
* Strong experience with CDISC, ADaM and SDTM
* Significant experience working in clinical trials phase I-IV
Please submit your application to find out more.
Jack Kavanagh
AL Solutions