Clinical Research Nurse Coordinator

ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY EMPLOYER. ALL QUALIFIED APPLICANTS WILL RECEIVE CONSIDERATION FOR EMPLOYMENT WITHOUT REGARD TO RACE, COLOR, RELIGION, SEX, SEXUAL ORIENTATION, GENDER IDENTITY OR EXPRESSION, NATIONAL ORIGIN, AGE, DISABILITY, PROTECTED VETERAN STATUS OR ANY OTHER CHARACTERISTIC PROTECTED BY FEDERAL, STATE, OR LOCAL LAWS.

This position has been designated as safety sensitive and cannot be filled by a candidate who is a current user of medical marijuana.

CURRENT EMPLOYEES: Please apply via the internal career site by logging into your Workday Account ( https://www.myworkday.com/archildrens/ )and search the "Find Jobs" report.

Work Shift

Day Shift

Time Type

Full time

Department

CC038145 Becton General

Summary

The Clinical Research Nurse Coordinator coordinates of clinical research studies. Serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study. The Clinical Research Nurse upholds standards for human subjects protection.

Additional Information

The Clinical Research Nurse Coordinator coordinates of clinical research studies. Serves as a resource for research study participants, families, other healthcare providers, and members of the clinical research team regarding specified aspects of the study. The Clinical Research Nurse upholds standards for human subjects protection.

Required Education

Associate Degree or Equivalent Experience

Recommended Education

Bachelor's Degree

Required Work Experience

Related Field - 3 years of experience

Recommended Work Experience

Required Certifications

Registered Nurse (RN) license - Arkansas or Compact State

Recommended Certifications

Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals, Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates

Description

1. Prepares materials for approval by ACRI and the applicable IRB.
2. Conducts screening procedures for study enrollment. Recruits subject for participation and obtains consent/assent for research participation.
3. Prepares flowcharts, study specific source documents and other study related materials.
4. Assures clinical interventions are administered per protocol.
5. Collects/records subject data on the case report forms using source documentation.
6. Serve as a clinical/research resource to subjects, families, and other healthcare providers regarding the needs of the study and subject/family.
7. Collaborates with other caregivers, research team members, and subject/family in planning, implementing, and evaluating research activities.
8. Performs other duties as assigned.