Central Monitoring Specialist

Remote • Posted 22 hours ago • Updated 22 hours ago
Contract W2
Contract Independent
Contract Corp To Corp
12 Months
No Travel Required
Remote
Depends on Experience
Fitment

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Job Details

Skills

  • Central Monitoring

Summary

Role: Clinical Data Analyst / Central Monitoring Specialist
Location: Remote (AZ, CA, DC, FL, GA, IA, IL, KS, MA, MD, NC, TN, VA, WV)
Duration: 6-Month Contract-to-Hire

 

 

Must Have:

  • 3+ years of Centralized Monitoring experience in a CRO or Clinical Research environment
  • Prior experience as a Clinical Research Associate (CRA)
  • Hands-on experience with:
    • Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs)
    • Central Monitoring Plans
    • Risk-Based Quality Management (RBQM)
    • Data dashboard review, signal detection, and risk analysis
  • Strong understanding of ICH-Google Cloud Platform and FDA regulations
  • Experience with clinical data systems, dashboards, Power BI, Tableau, SAS, SQL, R, or Python is a plus

Preferred:

  • Experience in Oncology, Infectious Disease, or Government-sponsored studies
  • Experience mentoring junior team members and improving monitoring processes

 

Responsibilities:

  • Develop and manage KRIs, QTLs, and centralized monitoring strategies
  • Review study data and dashboards to identify risks, trends, and compliance issues
  • Support risk assessments and site performance monitoring
  • Collaborate with Clinical Operations, Data Management, and Analytics teams
  • Maintain risk logs and recommend corrective actions
  • Support audits, inspections, and regulatory compliance
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10513292
  • Position Id: 72860-12895-
  • Posted 22 hours ago
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