Clinical Research Coordinator II - Pediatric Oncology

Carilion Clinic; Roanoke (VA); On-site; USD 45,000 - 63,000; Full time

Job summary

Carilion Clinic in Roanoke, Virginia is seeking a Clinical Research Coordinator II for Pediatric Oncology to coordinate studies, ensure regulatory compliance, and manage study operations in a fully in-person role.

You will recruit and enroll participants, obtain informed consent, maintain documentation, track adverse events, and liaise with sponsors, IRBs, and research teams while upholding quality and integrity of the trials.

Qualifications

• Bachelor’s degree required or 4 years of related experience.
• Minimum 2 years of healthcare or research experience.
• IATA certification required.
• Strong analytical and organizational skills.

Responsibilities

• Coordinate recruitment, screening, and enrollment of participants.
• Obtain informed consent and manage study documentation.
• Ensure compliance with study protocols and regulatory requirements.
• Collect, manage, and analyze study data.
• Maintain study databases and regulatory documentation.
• Track adverse events and protocol deviations.
• Communicate with sponsors, IRBs, and research teams.
• Support monitoring visits and audits.

Skills

Analytical skills

Organizational skills

Recruitment coordination

Education

Bachelor's degree

Job description

## Clinical Research Coordinator II - Pediatric OncologyApply: Fully In-Person: Roanoke, Virginia: Full time: Posted Today: End Date: October 30, 2026 (13 days left to apply): R162668## **Employment Status:**Full time## **Shift:**Day (United States of America)## **Facility:**1906 Belleview Ave SE - Roanoke## **Requisition Number:**R162668 Clinical Research Coordinator II - Pediatric Oncology (Open)# **How You’ll Help Transform Healthcare:**The Clinical Research Coordinator Pediatric Oncology coordinates clinical research studies and ensures compliance with regulatory requirements while managing study operations.The Clinical Research Coordinator Pediatric Oncology* Coordinates recruitment, screening, and enrollment of participants.* Obtains informed consent and manages study documentation.* Ensures compliance with study protocols and regulatory requirements.* Collects, manages, and analyzes study data.* Maintains study databases and regulatory documentation.* Tracks adverse events and protocol deviations.* Communicates with sponsors, IRBs, and research teams.* Supports monitoring visits and audits.# **What We Require:****Education:** Bachelor’s degree required or 4 years of experience may be considered in lieu of degree.**Experience:** Minimum 2 years of healthcare or research experience required.**Licensure, Certification, and/or Registration:** IATA required. Research certification preferred.**Other Minimum Qualifications:** Strong analytical and organizational skills.This job description is intended to be a representative summary of the major responsibilities and accountabilities performed by incumbents in this role. Incumbents may be requested to perform job-related tasks other than those specifically presented in this description.**Compensation Range:**$44,948.80 - $62,920.00*Employee pay is based on a variety of factors, including qualifications, credentials, education, and prior work experience. The compensation range does not include benefits or pension plan.***Recruiter:**RHONDA JOHNSON**Recruiter Email:**[e-mail]**For more information, contact the HR Service Center at 1-800-599-2537.**Carilion Clinic is an Equal Opportunity Employer: We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, national origin, age (40 or older), disability, genetic information, or veterans status. Carilion is a Drug-Free Workplace. For more information or for individuals with disabilities needing special assistance with our online application process contact Carilion HR Service Center at 800-599-2537, 8:00 a.m. to 4:30 p.m., Monday through Friday.