Clinical Program Manager

Axle Informatics

$140K — $150K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Master's degree required
  • SOCRA Certification preferred
  • FAC-P/M Certification preferred
  • FAC-COR Certification preferred
  • PMP Certification preferred
  • ACRP Certification preferred
  • Experience with clinical trial management systems and research databases

Responsibilities

  • Coordinate operational activities for clinical studies
  • Assist with feasibility assessments for proposed clinical trials
  • Support startup activities for new studies
  • Monitor study progress and metrics related to enrollment
  • Develop and maintain project management plans

Benefits

  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Various Flexible Spending Accounts (FSA)
Full Job Description
Axle is seeking a Clinical Program Manager to join our vibrant team at the National Institutes of Health (NIH) supporting the National Cancer Institute (NCI) located in Bethesda, MD.

Benefits We Offer:
  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Flexible Spending Accounts:
    • Healthcare (FSA)
    • Parking Reimbursement Account (PRK)
    • Dependent Care Assistant Program (DCAP)
    • Transportation Reimbursement Account (TRN)


Position Overview

The Contractor shall provide personnel capable of supporting complex clinical research portfolios and ensuring efficient coordination among investigators, research teams, oversight offices, regulatory agencies, collaborating institutions, and other stakeholders involved in the conduct of clinical research. Requires a Master's degree.

Additional Qualifications

Certifications & Licenses
  • SOCRA Certification
  • FAC-P/M Certification
  • FAC-COR Certification
  • PMP Certification
  • Association of Clinical Research Professionals (ACRP)

Field of Study
  • Health and Medical Administrative Services
  • Nursing

Software
  • Experience with clinical trial management systems and research databases

Skills
  • 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

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

Statement of Work Details
  • Coordinate operational activities for clinical studies - 1
  • Assist with feasibility assessments for proposed clinical trials - 2
  • Support startup activities for new studies - 3
  • Coordinate participating sites for multi-center trials - 4
  • Monitor study progress and enrollment-related metrics - 5
  • 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, Institutional Review Board (IRB) submissions, regulatory submissions, continuing reviews, study activation activities, and clinical trial monitoring activities
  • 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


Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.

This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.

Salary Range

$140,000-$150,000 USD

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