Clinical Research Project Manager II

Responsibilities

• Lead projects of varying complexity and size to support operational efficiencies across the Fred Hutch and Cancer Consortium clinical research enterprise.
• Scope projects, defining resources, stakeholders, and potential barriers with risk mitigation strategies.
• Convene cross-functional stakeholder meetings, tracking action items and key decisions to maintain progress.
• Establish, monitor, and communicate project plan and timelines, ensuring milestones are met.
• Manage internal and external stakeholders, fostering effective communication and collaboration.
• Develop, implement, and manage standard tools and processes to manage project requests and work closely with CRS leadership to maintain and vet prioritized project list, adjusting as appropriate.
• Create, update, and manage project deliverables including standard operating procedures (SOPs), process maps, templates, and guidance documents in support of implementation and change management of new system or processes.

Qualifications

• BA/BS in related field or equivalent experience. Minimum of four years project/study management experience with a master's degree or six years’ experience with a bachelor’s degree, in a research setting.
• Excellent written and verbal communication skills.
• Strong supervisory skills and budgeting experience.
• Grant and contract experience.