Mgr, Sr Programming I

Description Plans, organizes, and manages the activities of a Statistical Programming group in support of clinical projects across multiple therapeutic areas. Ensures all statistical programming functions meet ICH/GCP quality requirements in the support of product development and life cycle maintenance. Contributes to activities in statistical systems development, validation and implementation including Standard Reporting Systems, SAS macro utility programs and associated tools. Develops and oversees implementation of programming standards and conventions. Position Requirements Degree and experience in Computer Science, Statistics, or related field. At least eight (8) years of pharmaceutical experience with a masters degree or equivalent. At least six (6) years of pharmaceutical experience with a Ph.D. degree or equivalent. Four to six years of leadership role in a technical and/or statistical programming environment in a pharmaceutical or biotechnology environment. Minimum of two years in a management position in a multi project environment with resource, timeline and budgetary responsibilities. Project Management experience in a global clinical trial environment. Experience in the development and implementation of global statistical programming standards and conventions. Excellent knowledge of clinical trial methodology and emerging global programming and data interchange standards. Demonstrated technical abilities and skills particularly in statistical software packages (e.g. SAS, S Plus). Ability in programming system development and validation. Leadership, analytical, problem solving and technical skills. Demonstrated organizational, verbal, written and interpersonal skills. Excellent ability to work on multiple projects with competing priorities. Ability to travel 5 to 10 percent. Apply for this Job