Senior statistical programmer - SA Bench at Cytel

• Working under the direction of the Principal Programmer, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities.
• Lead at least one study team in terms of providing technical and domain-related guidance.
• May require to lead and manage a team of 2-4 members
• Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard.
• Read and understand the program specifications document.
• Prepare SAS analysis datasets, tables, listings, and figures as per specifications.
• Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery.
• Validate and transform datasets as per client assignment specifications.
• Validate tables, listings, and figures as per client assignment specifications.
• Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
• Contribute to the organization’s recruitment process by identifying needs and required skill set of resources and conducting interviews to hire appropriate resources.
• Perform all the above tasks using standard operating procedures (SOPs) as defined in Quality Management System or the respective client(s) as applicable

Qualifications and Experience:

• Bachelors or Masters's degree in Computer Science, Statistics, or related health science field with 5 plus years of SAS programming experience with clinical trial data.
• CDISC experience is required.
• Well conversant with regulatory requirements and drug development process.
• Good understanding of the Clinical trial domain and good SAS programming skills
• Ability to work independently.