Cancer Center Jobs

Clinical Research Project Manager II
Job ID: 30789
Type: Regular Full-Time
Location: US-WA-Seattle

Please apply to this role at: https://careers-fhcrc.icims.com/jobs/30789/clinical-research-project-manager-ii/job

Overview
Fred Hutch Cancer Center is an independent, nonprofit organization providing adult cancer treatment and groundbreaking research focused on cancer and infectious diseases. Based in Seattle, Fred Hutch is the only National Cancer Institute-designated cancer center in Washington.

The Clinical Research Project Manager II will lead a diverse portfolio of projects to enhance operational efficiencies in the administration and management of the Fred Hutch and Cancer Consortium clinical trials. The Project Manager reports into the central clinical trials office, Clinical Research Support, and manages internal and external collaborations across multiple teams and departments and drives decisions to ensure project milestones and deliverables are met in an efficient manner. This role will be responsible for self-directing large, complex projects from initiation to completion. The role will be responsible for defining project scope, resources, and stakeholders, identifying technical solutions, and will work closely with CRS leadership to develop project deliverables that may include standard operating procedures (SOPs), tools, workflows, and process maps. This position requires flexibility in a dynamic environment to ensure the prioritization of projects is aligned with departmental and institutional strategic goals.

This role will have the opportunity to work partially at our campus and remotely, and will need to be present on-campus as needed for projects.

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
• Provide document management and version control of all project-related materials

Minimum 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

Preferred Qualifications

• MA/MS desired
• Oncology clinical research experience in an academic setting
• Clinical study coordinator or other clinical research management experience
• Research systems workflow experience
• Demonstrated ability to successfully self-direct projects from initiation to completion
• Demonstrated excellent human relations, facilitation and influencing skills to deal effectively with all levels of employees and management
• Ability to effectively create and execute project steps toward desired end results
• Ability to quickly synthesize complex issues to move project forward
• Knowledge of clinical protocol development, review and approval process

The annual base salary range for this position is from $88,712 to $133,058, and pay offered will be based on experience and qualifications. This position may be eligible for a sign-on bonus.