Full-time
Clinical Research Coordinator
$73K/yr – $84K/yr
Winchester, VAScience & PharmaceuticalPosted 17d ago
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Role overview
Job type
Salary
$73K/yr – $84K/yr
Location
Sector
Posted
17 days ago
Job description
Responsibilities
Screens potential participants for protocol eligibility
Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials
Coordinates participant care in compliance with protocol requirements
May disburse investigational product and maintain accountability records
Oversees preparation of orders by providers to ensure protocol compliance
Packages and ships laboratory specimens to central vendors as applicable
Completion of Hazmat and/or IATA training may be required
In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment
Thoroughly document all findings and participate in data collection
Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports
Maintains regulatory documents in accordance with organizational SOPs and applicable regulations
May assist with scheduling monitoring and auditing visits and interact with monitors/auditors as needed
May collaborate with research leadership in study selection processes
Participates in required training and education programs
May contribute to education of clinical staff regarding research procedures
Works with staff to develop action plans and improvement initiatives to enhance quality
May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers
May review protocol‑specific billing guides and submit billing information to the appropriate personnel
Other duties as assigned
Preferred
Bachelor's degree preferred
Oncology clinical research experience strongly preferred
Demonstrated experience independently obtaining informed consent, coordinating participant visits, managing regulatory documentation, reporting adverse events, and supporting sponsor monitoring visits preferred
SoCRA (CCRP) or ACRP certification preferred
Benefits
Full-Time | Onsite | Monday – Friday
Employees are valued, supported, and empowered to grow
Professional growth opportunities
Every day, The US Oncology Network helps approximately 3,300 providers deliver value-based, integrated care for patients—close to home.
The Woodlands, Texas, USA
http://www.usoncology.com/
Late Stage
Total Funding
unknown
2010-12-30
Acquired
Recent News
Business Wire
Research Presented by The US Oncology Network Demonstrates How Community Practices Are Expanding Patient Access Through APP‑Led Models at ASCO 2026
2026-05-29
PR Newswire
29 Physicians from Virginia Cancer Specialists Named to Washingtonian Magazine's Top Doctors List 2025
2025-10-27
DeepScribe Solidifies Ambient AI Leadership in Oncology with New Study and Accelerated Growth
2025-09-17
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Qualifications
Associate's degree in a clinical or scientific discipline required, or an equivalent combination of education, clinical research experience, and applicable certification
Minimum three years of Clinical Research Coordinator experience in a clinical research setting required
Bachelor's degree preferred
Oncology clinical research experience strongly preferred
Demonstrated experience independently obtaining informed consent, coordinating participant visits, managing regulatory documentation, reporting adverse events, and supporting sponsor monitoring visits preferred
SoCRA (CCRP) or ACRP certification preferred
Minimum three years of Clinical Research Coordinator experience in a clinical research setting required.
Required skills
Clinical Research Coordination, Oncology Clinical Research, Informed Consent, Participant Visit Coordination, Regulatory Documentation, Adverse Event Reporting, Sponsor Monitoring Visits, SoCRA (CCRP) Certification, ACRP Certification
Preferred skills
Bachelor's degree preferred, Oncology clinical research experience strongly preferred, SoCRA (CCRP) or ACRP certification preferred
Experience
3+ years
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