Regulatory Affairs Coordinator, Human Subjects Research

Arkansas Children's Hospital; Little Rock (AR); On-site; USD 65,000 - 95,000; Full time

Job summary

Arkansas Children's Hospital is seeking a Regulatory Affairs professional to oversee regulatory activities for research within the Arkansas Children's Research Institute. You will ensure protocols involving human subjects comply with federal regulations, state codes, IRB oversight, and institutional policies.

Responsibilities include preparing IRB submissions, coordinating regulatory documentation, and ensuring ongoing compliance with training requirements and sponsor expectations.

Qualifications

• High School Diploma/GED required.
• Bachelor’s degree recommended in a related field.
• Certified Clinical Research Professional (CCRP) certification recommended.

Responsibilities

• Prepare and submit IRB documents under the PI/Research Administrator’s direction.
• Review start-up regulatory forms and related documents for sponsor/IRB compliance.
• Coordinate pre-site visits and site initiation visits with protocol planning.

Education

High school diploma or GED or equivalent

Bachelor’s degree in a related field

Certified Clinical Research Professional (CCRP)

Job description

Arkansas Children's Hospital is seeking a Regulatory Affairs professional to oversee regulatory activities for research within the Arkansas Children's Research Institute. You will ensure protocols involving human subjects comply with federal regulations, state codes, IRB oversight, and institutional policies.

Responsibilities include preparing IRB submissions, coordinating regulatory documentation, and ensuring ongoing compliance with training requirements and sponsor expectations.