Statistical Programmer

The Statistical Programmer provides support to the lead programmer and the study team on all programming activities according to the study requirements and the timelines. The incumbent implements and performs the programming and project standard under general supervision of the lead programmer and manager to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. In this role, a typical day might include the following:

• Provide programming support within multiple studies/projects in various study activities with timely and high-quality programming results in assigned tasks and projects
• Work with lead programmer and manager in cross-functional collaborations to support the study conduct and reporting activities.
• Maintain all documentation in accordance with SOPs/Guidance/WI/process to ensure traceability and regulatory compliance
  
  Proficiency in SAS. Knowledge of other programming languages such as R, Python etc.
• Good knowledge of pharmaceutical clinical development (i.e., understanding of statistical concepts, techniques, and clinical trial principles)
• Ability to work on global interdisciplinary teams. Good organizational, interpersonal, and communication skills. Positive attitude, standout colleague and growth mindset
To be considered for this opportunity you will need: MS. (BS) in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related discipline with 1+ (2+) years of programming experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. SAS Certification a plus. #GDBDMJobs