- Work under the direction of the Principal Programmer.
- Conduct programming activities for a trial, early phase project, indication, or publication activities.
- Lead at least one study team, providing technical and domain-related guidance.
- May require leading and managing a team of 2-4 members.
- Perform data migration from legacy datasets to standards such as CDISC or any other client-specific standard.
- Read and understand program specifications documents.
- Prepare SAS analysis datasets, tables, listings, and figures as per specifications.
- Create programs to generate graphs and tables 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 on specifications, data issues, outliers, reviews, schedules, etc.
- Contribute to the organization s recruitment process by identifying needs, determining the required skill set of resources, and conducting interviews to hire appropriate resources.
- Perform all tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable.
Qualifications and Experience:
- Bachelors or Masters degree in Computer Science, Statistics, or a related health science field.
- 5+ years of SAS programming experience with clinical trial data.
- CDISC experience is required.
- Well-versed in regulatory requirements and the drug development process.
- Good understanding of the clinical trial domain and strong SAS programming skills.
- Ability to work independently.
