Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research Associates, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines for statistical data analysis and reporting.
February 25, 2020
Provide tactical support for the timely preparation, editing and review of submissions, including regulatory agency Meeting Requests and Briefing Documents, IND/CTA amendments, original Marketing Authorization Applications and their respective amendments/supplements.
March 30, 2020
Review and approve all Product development documents, Master Formula, Batch Manufacturing records, Validation protocols and reports.
April 16, 2020
Assist in development endeavors including meetings with potential donors, recruiting new supporters through personal contacts, and working with development staff on program narrative for grants and other fund-raising responsibilities including the annual gala, the Bear Affair.
May 01, 2020
Participate in the revision of the annual application review guide and publications (Common Application, Slate application, etc), assisting to direct efforts of both colleagues within admissions and those from other departments such as faculty.
May 20, 2020
Demonstrated cultural fluency with all constituencies including students, families, and college admission professionals from a range of diverse ethnic and socioeconomic backgrounds.
May 23, 2020
Creates an innovative environment where strong professional practice flourishes and the mission, vision and values promote positive patient outcomes believed to be important for the organization.
June 19, 2020