Clinical Research Coordinator II - Mental Health

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

Job summary

Carilion Clinic in Roanoke, Virginia, invites applications for a Clinical Research Coordinator II focused on Mental Health. The role coordinates studies, screens participants, and ensures regulatory compliance, working closely with sponsors, IRBs, and research teams.

Ideal candidates have a bachelor’s degree or equivalent experience, at least two years in healthcare or research, and IATA certification. The position is in-person at 2017 S Jefferson St, offering day shifts and a competitive salary.

Qualifications

• Bachelor's degree required, or 4 years of experience in lieu.
• Minimum 2 years of healthcare or research experience.
• IATA certification required; research certification preferred.
• Strong analytical and organizational skills.

Responsibilities

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

Skills

Analytical skills

Organizational skills

Education

Bachelor's degree

Job description

## Clinical Research Coordinator II - Mental HealthApply: Fully In-Person: Roanoke, Virginia: Full time: Posted Today: End Date: October 30, 2026 (13 days left to apply): R163181## **Employment Status:**Full time## **Shift:**Day (United States of America)## **Facility:**2017 S Jefferson St - Roanoke## **Requisition Number:**R163181 Clinical Research Coordinator II - Mental Health (Open)# **How You’ll Help Transform Healthcare:**The Clinical Research Coordinator coordinates clinical research studies and ensures compliance with regulatory requirements while managing study operations.The Clinical Research Coordinator* 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.