Overview
We are seeking a Senior Statistical Programmer to join a global pharmaceutical company on a contract basis. This remote position invites candidates from the UK and Europe to utilize their advanced R programming skills to support the analysis and reporting of unblinded clinical trial data, while working closely with cross-functional teams in a dynamic environment.
Responsibilities
- Develop statistical programming solutions for clinical trial data analysis.
- Collaborate with clinical teams to produce safety and efficacy outputs.
- Generate complex graphical representations of data using R.
- Monitor data for safety and adverse events reporting.
- Prepare documentation for regulatory submissions and respond to queries from authorities.
- Ensure proper access controls and confidentiality of unblinded data.
Requirements
- Minimum of 5 years experience in statistical programming or a related field.
- Advanced proficiency in R programming with experience in graphical output generation.
- Strong understanding of statistical methodologies for clinical trials.
- Experience in creating safety and efficacy tables, listings, and graphs.
- Familiarity with regulatory submission processes.
- Experience with unblinded data handling and appropriate access controls is preferred.