Manage one or more (depending on size/scale) clinical trial related process improvement projects from inception to project closure.
Support an assigned Project Lead and team of Subject Matter Experts with regular meeting management, project planning/timeline management, coordination of implementation plan components, resource tracking, and communication/change management planning.
Proficient in MS Project, PowerPoint, and Excel is mandatory.
Manages one or more high-level, complex non-technical projects within the constraints of scope, quality, time, and cost, to deliver specified requirements.
Projects may be strategic in nature.
Responsibilities may include resource allocation and all phases of development life cycle (i.e. feasibility study, requirements, analysis, ROI, business plan, design, testing, and implementation planning).
Regularly interacts with management.
Coordinates and directs the activities of project team members.
May be responsible for cross-functional teams.
Ensures all project requirements and/or objectives are documented.
May obtain and manage external resources required for project completion.
Expertise in running medium to large scale projects
Excellent understanding of project management processes and procedures
Experience with project management and analyst methodologies and best practices
Strong analytical skills ; business process development best practices, change management
Strong MS Project, MS Word, Visio, MS PowerPoint and MS Excel skills
Understanding of systems for sharing and collaboration
Excellent communication skills to work with cross-program resources
Preferred 5+ years of Project Management experience.
"This posting is for Contingent Worker, not an FTE"