Mgr, Clinical Trials Proj (L)

Responsibilities

• Leads and oversees the Project Management Team for the URCC NCORP Research Base
• Supervises the Project Management team and oversees project coordination across the Research Base clinical trial portfolio
• Ensures PMs maintain accurate timelines, action logs, milestone trackers, and study-specific operational plans
• Identifies barriers, timeline risks, resource constraints, and operational issues; works with Assistant Director to resolve or escalate as needed
• Ensures PM work aligns with NCI expectations, Research Base priorities, and cross-functional team workflows
• Works closely with Research Base leadership, Study Chairs, cross-functional operational teams, and external collaborators to ensure project management activities are timely, coordinated, compliant, and aligned with Research Base priorities

Requirements

• Bachelor's degree and 6 years of relevant experience required
• Master's degree preferred
• Previous leadership experience required
• Extensive knowledge of protocol planning, implementation, coordination, evaluation, and reporting of clinical trials required
• Strong communication skills, interpersonal skills, attention to detail, and organization skills required

Qualifications

• CITI Human Subject Protections and Good Clinical Practice Certifications required upon employment
• CCRP - Certified Clinical Research Professional upon hire preferred
• Certified Project Management Professional (PMP)-PMI upon hire preferred