The Associate Director/DGM, Statistical Programming will play a pivotal role in providing comprehensive programming expertise to lead and support all programming activities as per the project strategies along with managing a large team of programmers in successful and timely completion of all programming activities for highly complex studies and regulatory submissions. The incumbent should be able to work independently implementing and executing the programming and project standards to support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc analysis. The incumbent will work closely with internal partnering functions, stakeholders, and external functional service providers to ensure all the programming deliverables are delivered in timely manner with high quality. The incumbent will participate in and contribute to department goals, SOPs, macros, SME topics and act as a technical expertise to provide guidelines on CDISC standards.