[Remote] reputed company Project Manager, Clinical Trials
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, Clinical Trials with hands-on oncology clinical trials leadership experience to reputed company the planning, coordination, and execution of clinical trials workstreams reputed company a reputed company reputed company transformation program.
Responsibilities
- reputed company end-to-end project management of oncology clinical trials workstreams, including planning, scheduling, execution, monitoring, and closeout
- reputed company and maintain comprehensive project plans, trial timelines, risk registers, and status reporting for clinical trials 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 clinical trials-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 clinical trials 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 clinical trials 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 clinical trials activities
Skills
- MD, RN, or reputed company Practitioner (NP) required
- 5+ years of reputed company experience leading oncology clinical trials, 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 Public 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