Our client, a global pharmaceutical leader, seeks a highly skilled Senior Statistical Programmer to drive innovation in patient treatment.
This key role involves leveraging advanced SAS skills and CDISC proficiency to support or lead clinical trials, working remotely with autonomy and ownership.
Key to success are our core values :
- Delivering scientific excellence through data-driven insights.
- Nurturing curiosity and enthusiasm for innovative problem-solving.
- Collaborating across diverse perspectives to unlock new possibilities.
- Embracing cutting-edge technology to deliver intelligent solutions.
Responsibilities
Contribute by :
Executing data manipulation, analysis, and reporting using SAS programming.Generating and validating SDTM and ADaM datasets / tables utilizing raw data.Developing production and QC / validation programming.Creating ad-hoc reports to meet client needs.Applying strong efficacy analysis understanding and experience.Reviewing submission documents and eCRTs.Communicating project specifications, status, and issues to internal teams and clients.Leading duties when called upon and serving as a team player meeting deadlines.Qualifications
Success requires : Bachelor's degree in Statistics, Computer Science, Mathematics, or related field. A minimum of 8 years of SAS programming experience with clinical trial data is necessary. Study lead experience is preferred.