Sr. SAS Programmer

Responsibilities :

• The Sr. SAS Programmer will be responsible for statistical programming for the client's clinical studies.
• In this role, you will develop and validate SAS programs for data presentation, analyses, and provide programming support to project team members.
• Our Ideal candidate will have a strong work ethic capable of thriving in a high growth, fast paced and intellectual environment.
• Serves as lead programmer for assigned projects to provide statistical and programming support in one or more Phase I-III clinical studies.
• Design and perform quality checks on analysis datasets, tables, listings, figures (TFL), and written reports to support clinical trial results using SAS.
• Create and review annotated CRF to STDM datasets.
• Produce and maintain technical programming specification documents.
• Lead and actively participate in client and project review meetings.
• Communicate with clients regarding study protocol or statistical analysis issues.
• Validate statistical deliverables and ensure that appropriate statistical methods are utilized.
• Ensure adherence to industry standards and regulatory requirements.
• Facilitate the development and application of adequate statistical methods in clinical research.

Requirements :