Clinical trials are high stakes, demanding high standards. Veramed sets this standard by bringing together the sharpest minds in data management, biostatistics and programming, with cutting-edge technology and proven processes.
Our globally connected, caring team delivers quality, precision and collaboration, earning trust through consistency and integrity. From rapid-fire project work to long-term partnerships, Veramed brings the right minds to every challenge.
We have exciting Immediate contract opportunities available for Senior or Principal level Statistical Programmers in the UK to work with Veramed.
Do you have any of the following skillsets? if so, please reached out detailing your experience of any of the below:
* In-depth Study Lead experience - Skilled in leading studies and SAS expertise.
* R Programming skills - Previous experience of working in R and ability to help deliver training.
* Macro Development expertise - In-depth experience in creating, maintaining, and governing Macros.
ADDITIONAL REQUIREMENTS:
* Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs.
* Author and review simple and complex study TFL shells.
* Author and review simple and complex dataset standards.
* Perform data checks and data exploration (e.g. using frequencies, histograms).
* Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice.
* Complete and review CDISC Validation tool reports.
* Ensure the appropriate standards are being applied and adhered to.
* Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival).
* Review of project management related documents.
* Maintain study master file documents and any other documents that are required to be audit ready.
Please use the link to apply or if you wanted to have a chat feel free to reach out to me at jon.gibbs@veramed.com or via LinkedIn.