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Statistical Programmer - Contract

Statistical Programmer - Contract

RBW Consulting
30+ days ago
Job type
  • Remote
Job description

Job Summary : We are seeking a highly skilled and experienced Statistical Programmer to join our client's dynamic team. The successful candidate will play a critical role in the programming and analysis of clinical trials and other research studies, with a specific focus on diabetes. This position requires strong programming skills, attention to detail, and the ability to work collaboratively with cross-functional teams. The role offers a hybrid working arrangement, requiring onsite presence in the San Francisco area.

Key Responsibilities :

  • Programming : Develop and maintain SAS programs to analyze clinical trial data, generate tables, listings, and figures, and create datasets.
  • Data Management : Collaborate with data management teams to ensure accurate and efficient data collection, cleaning, and validation processes.
  • Statistical Analysis : Support biostatisticians in performing complex statistical analyses by providing well-documented and validated programs.
  • Study Design : Assist in the design of clinical trials and observational studies, including the development of statistical analysis plans.
  • Reporting : Prepare detailed statistical reports, including summary statistics, inferential statistics, and graphical representations of data.
  • Collaboration : Work closely with clinical researchers, data managers, and other stakeholders to provide programming expertise and support throughout the study lifecycle.
  • Regulatory Compliance : Ensure all programming activities comply with regulatory requirements and guidelines, including GCP, ICH, and FDA standards.
  • Documentation : Maintain thorough documentation of programming activities, including program specifications, validation plans, and user guides.

Qualifications :

  • Education : Bachelor’s or Master’s degree in Statistics, Computer Science, or a related field.
  • Experience : Minimum of 5 years of experience in statistical programming, with direct experience in diabetes research or clinical trials.
  • Skills : Proficiency in SAS programming, strong analytical and problem-solving skills, excellent written and verbal communication skills.
  • Knowledge : In-depth knowledge of clinical trial design, statistical methodologies, and regulatory requirements.