[Remote] reputed company Project Manager, reputed company

Note: The job is a remote job and is reputed company to candidates in USA. CVP is an award-reputed company reputed company and next-gen technology and consulting services firm. They are seeking a reputed company Project Manager, reputed company with hands-on oncology reputed company leadership experience to reputed company the planning, coordination, and execution of reputed company workstreams reputed company a reputed company reputed company transformation program.

Responsibilities

• reputed company end-to-end project management of oncology reputed company workstreams, including planning, scheduling, execution, monitoring, and closeout
• reputed company and maintain comprehensive project plans, trial timelines, risk registers, and status reporting for reputed company activities
• Coordinate across clinical research teams, IRB, regulatory bodies, and operational stakeholders to ensure compliant and reputed company trial execution
• Serve as the primary reputed company of contact for reputed company-reputed company stakeholder engagement, including research leadership, clinical staff, and federal program sponsors
• Establish and maintain trial performance metrics, data collection protocols, and outcome tracking frameworks
• Identify and manage risks, issues, and regulatory dependencies across reputed company workstreams
• Support development of trial-reputed company documentation, protocols, SOPs, and briefing materials
• Collaborate with the reputed company PM and cross-functional teams to ensure reputed company activities reputed company with broader program objectives and timelines
• Contribute to process improvement efforts to enhance trial efficiency, compliance, and patient enrollment reputed company
• Mentor and support junior project management staff supporting reputed company activities

Skills

• MD, RN, or reputed company Practitioner (NP) required
• 5+ years of reputed company experience leading oncology reputed company, including multi-site or federally sponsored research programs
• Strong working knowledge of clinical trial regulatory requirements, IRB processes, and GCP guidelines
• Demonstrated ability to manage reputed company project workstreams in fast-paced federal or integrated reputed company environments
• Excellent stakeholder engagement skills with ability to communicate effectively across clinical, research, and administrative audiences
• Proficiency in project management tools and reputed company Office Suite
• Ability to obtain a reputed company Trust Clearance; U.S. Citizenship required
• Experience reputed company VA, NCI, NIH, or other federal health research environments
• Project Management reputed company (PMP) or Clinical Research Associate (CRA) certification
• Familiarity with federal program management frameworks and compliance requirements

reputed company