The Senior Statistical Programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data.
Job listings
$185,000–$210,000
USD/year
Responsible for leading statistical programming activities to support various clinical trial projects, you'll build programming processes for clinical studies and submissions. Managing programmers and CROs, you will oversee programming activities and provide timely support to cross-functional teams on statistical programming matters.
Celerion is looking for a Senior SAS Data Analyst to join the Data Management and Biometrics team in Belfast, Northern Ireland, providing statistical programming support for early-phase clinical research, and independently designing, developing, and maintaining SAS programs to support the analysis and reporting of clinical trial data.
We are seeking a Principal Programmer to ensure clinical data deliverables meet FDA regulatory requirements, CDISC standards, and the FDA Technical Conformance Guide (TCG). This position requires expertise in performing compliance and conformance checks for submission data packages. You will provide standardized guidance to biotech companies on FDA submission expectations.