Senior Statistical Programmer
Responsibilities :
- Working under the direction of the Team Lead / Project Manager, 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 required to lead and manage a team of 2-4 members.
- Experience of working on Oncology TA is mandatory.
- 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 in the organization's recruitment process by identifying needs and required skill sets of resources and conducting interviews to hire appropriate resources.
- Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable.
Requirements :
- BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data.
- Well-conversed with regulatory requirements and drug development process.
- Good understanding of the Clinical trial domain and good SAS programming skills.
- Ability to work independently.
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