Job Description

About the Role

Our client is seeking a Sr. Clinical Research Coordinator to support Hematology/Oncology clinical trials within a pediatric healthcare setting. This is a fully onsite position located on the main corporate campus and is ideal for an experienced research professional who is comfortable managing high-enrollment studies and complex clinical trial activities.

The Sr. Clinical Research Coordinator will independently manage the day-to-day operations of assigned studies while ensuring compliance with study protocols, GCP guidelines, IRB requirements, and FDA regulations. This role will work closely with investigators, sponsors, CROs, research staff, and multidisciplinary healthcare teams to support successful study execution.

Key responsibilities include:

• 
  Coordinate and manage Hematology/Oncology clinical trials
• 
  Support patient recruitment, screening, enrollment, and follow-up
• 
  Maintain accurate study documentation, patient records, and regulatory files
• 
  Coordinate specimen collection, processing, and shipment activities
• 
  Manage study data within CTMS and research systems
• 
  Schedule and facilitate monitor visits and investigator meetings
• 
  Communicate with sponsors, CROs, investigators, and research teams regarding study progress
• 
  Monitor enrollment goals and support high-volume research activity
• 
  Maintain audit readiness and e-regulatory documentation
• 
  Assist with mentoring and training junior research staff
• 
  Support process improvement and operational research initiatives

Requirements

Qualifications

• 
  Bachelor's Degree with 4+ years of clinical research experience
  
  OR
• 
  Associate's Degree with 6+ years of clinical research experience
  
  OR
• 
  7+ years of clinical research experience

Required Experience

• 
  Strong knowledge of:
  • 
    Clinical trial protocols
  • 
    Good Clinical Practice (GCP)
  • 
    IRB processes
  • 
    FDA regulations
• 
  Experience coordinating Oncology or Hematology clinical research studies
• 
  Experience supporting patient enrollment and study documentation
• 
  Experience with CTMS, e-regulatory systems, and research databases
• 
  Ability to manage multiple studies and priorities simultaneously
• 
  Strong organizational, communication, and problem-solving skills

Preferred Background

• 
  Pediatric clinical research experience
• 
  Oncology or Hematology research experience
• 
  Interventional clinical trial experience

Additional Information

• 
  Fully onsite position
• 
  Opportunity to support high-impact pediatric oncology research programs