The Senior Biostatistician will provide statistical support for clinical studies, including protocol development, sample size calculations, and the creation of statistical analysis plans. They will also perform statistical analyses, interpret results, and prepare clinical study reports to support regulatory submissions.
The Principal Biostatistician will lead Phase I-IV clinical studies and provide strategic statistical guidance for clinical development plans and protocols. They will also perform complex statistical analyses, utilize machine learning algorithms, and ensure the integrity of data through rigorous review and reporting.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials while ensuring compliance with CDISC standards. They will also lead project tasks, generate submission documents, and collaborate with cross-functional teams to meet project deadlines.
The Senior Statistical Programmer will perform data manipulation, analysis, and reporting for clinical trials using SAS while ensuring compliance with CDISC standards. They will also lead project tasks, validate datasets, and communicate effectively with cross-functional teams and clients.
The Principal Statistical Programmer implements reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They are also responsible for overseeing CRO programmers to ensure high-quality and consistent data summaries.
Lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. The role involves working embedded within a pharmaceutical client to deliver high-quality data manipulation and reporting.
