As the Director of Statistical Programming within the Analytics and Data Sciences (ADS) team, you will lead the global statistical programming department, driving strategy and execution across all stages of drug development. You will manage resources to ensure study, program, and therapeutic area milestones are met, collaborating with various departments to align strategies and uphold quality standards. Your role is pivotal in developing operational strategies for statistical programming, fostering partnerships with external vendors, and enhancing internal processes. By implementing best practices and innovation in data standards and statistical reporting, you will significantly contribute to the success of our drug programs and the advancement of our development sciences. As a senior leader, you will empower your team through coaching and advocacy, facilitating a culture of excellence and continuous improvement. What You’ll Do: Develop and implement operational and sourcing strategies for statistical programming and data standards. Lead the management of statistical programming vendor relationships and strategic partnerships. Ensure timely execution of statistical programming and electronic submission activities across all drug programs. Identify opportunities for technical and process improvements and drive implementation. Develop and oversee programming standards, conventions, and efficient procedures. Provide leadership in talent acquisition, retention, and development within the department. Collaborate with cross-functional teams to align strategies and ensure optimal data delivery and analysis. Manage resources and budgets effectively to meet program goals. Stay updated on regulatory requirements and trends to ensure compliance. Promote a culture of innovation and continuous improvement within the team. Who You Are: You are a visionary leader with a strategic mindset and a passion for driving excellence in statistical programming. Your strong collaboration skills enable you to build effective partnerships and influence without authority. You possess a deep understanding of regulatory requirements and a commitment to maintaining high-quality standards. Your ability to manage complex projects and navigate cross-functional initiatives makes you an asset to any team. You thrive in a dynamic environment where you can inspire and develop others to achieve their full potential. Required Skills: Bachelor’s degree required; Masters or PhD in Statistics or Mathematics preferred. 12 years of relevant work experience in data management and analysis. 12 years of SAS Base programming experience, with 7 years using SAS STAT, GRAPH, and MACRO. 12 years of relevant industry experience and clinical trial experience. 7 years of clinical database experience. 7 years in a supervisory role. Extensive knowledge of regulatory requirements and drug submission guidelines. Strong management and leadership skills with the ability to lead cross-functional teams. Proven ability to manage multiple priorities and drive process improvements. Excellent written and oral communication skills. Preferred Skills: Experience with strategic change management within a large cross-functional initiative. Strong skills in compelling communication, driving execution, and cultivating networks. Job Level: Management.