# Clinical Program Manager

**Company:** [Axle](https://hotfix.jobs/companies/axle)
**Location:** Bethesda, MD
**Role:** Technical Program Management
**Salary:** $140k – $150k/yr
**Experience:** 5+ years
**Skills:** clinical research, Project Management, clinical trial management, Regulatory Compliance, Risk Management, Budget Management, pmp, socra, acrp, irb submissions, protocol development, nih experience
**Posted:** 2026-07-20

> Oversee and coordinate complex clinical research portfolios for the National Cancer Institute at NIH. Manage timelines, budgets, regulatory compliance, risks, and stakeholder communications for multi-center trials.

## Job Description

## Deliverables
- Monthly Activity Report
- Portfolio Status Report
- Risk Management Report
- Financial Status Report
- Regulatory Tracking Report
- Strategic Planning Support Reports (Ad-Hoc)
- Annual Program Summary Report
- Final Contract Summary Report (Ad-Hoc)

## Responsibilities
- Coordinate operational activities for clinical studies
- Assist with feasibility assessments for proposed clinical trials
- Support startup activities for new studies
- Coordinate participating sites for multi-center trials
- Monitor study progress and enrollment-related metrics
- Facilitate communication among study stakeholders
- Provide comprehensive management and oversight of assigned clinical research portfolios
- Develop and maintain project management plans for clinical research projects
- Monitor project schedules, timelines, deliverables, dependencies, and milestones
- Track portfolio performance metrics and report progress to leadership
- Assist Branch Chiefs and Program Leadership in prioritization of research activities
- Support portfolio planning and resource allocation efforts
- Monitor project execution to ensure alignment with organizational objectives
- Lead development and maintenance of project-specific work plans
- Coordinate project initiation, planning, execution, monitoring, and closeout activities
- Facilitate project meetings and maintain meeting documentation
- Track action items and follow-up activities
- Monitor project performance and identify potential barriers to success
- Assist investigators and research teams in achieving project objectives
- Develop risk mitigation and response plans
- Monitor identified risks throughout the project lifecycle
- Escalate significant issues to leadership as appropriate
- Coordinate corrective actions and resolution activities
- Identify operational, regulatory, financial, and programmatic risks
- Monitor and coordinate activities associated with protocol development, protocol amendments, IRB submissions, regulatory submissions, continuing reviews, study activation, and clinical trial monitoring
- Support preparation for audits, inspections, and monitoring visits
- Coordinate activities among investigators, regulatory staff, data managers, and clinical teams
- Monitor compliance-related milestones and deliverables
- Facilitate timely submission of required regulatory documents
- Assist with development of project-specific budgets
- Monitor expenditures and financial performance
- Track project funding and resource utilization
- Develop financial forecasts
- Identify potential budgetary concerns and recommend corrective actions
- Prepare financial status reports for leadership review
- Serve as liaison between assigned research programs and the Office of the Clinical Director (OCD), NCI Technology Transfer Center, regulatory offices, collaborating institutions, industry partners, and other NIH and NCI organizations
- Coordinate leadership briefings and status updates
- Prepare communication materials and project summaries
- Assist Government personnel with development of Statements of Work
- Assist with technical evaluations and acquisition planning activities
- Track contractor performance, deliverables, and invoice status
- Monitor contract milestones and option periods
- Support COR activities as requested
- Support strategic planning initiatives
- Analyze program performance and operational effectiveness
- Develop recommendations for process improvements
- Assist leadership with prioritization of future research initiatives
- Support implementation of organizational best practices

## Requirements
- Master's degree
- SOCRA Certification
- FAC-P/M Certification
- FAC-COR Certification
- PMP Certification
- ACRP Certification
- Experience with clinical trial management systems and research databases
- Experience with technology transfer agreements, clinical trial agreements, cooperative research and development agreements, or related research partnerships
- Experience supporting NIH, NCI, academic medical centers, or federally funded research programs

## Nice-to-Haves
- Field of Study in Health and Medical Administrative Services or Nursing

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