Research Monitoring Specialist
Arkansas Children's
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- Location
- Little Rock, United States
- Work style
- On-site
- Job type
- Full time
- Posted
- Oct 22
- 2 days ago
Career path
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About the company
Arkansas Children's
Hospital & health care · 1,001 to 5,000 employees
What you'll do
- Develop, implement, and maintain a monitoring program and tools for human research
- Obtain documents and assure the files are complete
- Conduct initial, interim and close-out monitoring visits for designated studies
- Communicate issues, monitoring status, potential findings, and education opportunities
- Review contracts for required elements
- Develop procedures, tools, trend analyses, and quality improvement efforts
- Assist in educational activities and training, coordinate audit trends, and be a content resource
- Assist research project development, drafting forms, and reviewing documents
What you need
- High school diploma or GED or equivalent
- 2 years of relevant experience, or 4 years of experience in lieu of a diploma/GED
- Bachelor's degree in a related field of study (preferred)
- SOCRA CCRP certification or ACRP-CP certification (preferred)
Key skills
SOCRA CCRP certificationACRP-CP certificationmonitoring activitiescompliance
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Read the full posting here
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:
CC033007 Research Integrity
Summary:
Responsible for monitoring activities to assure compliance. Provides reviews of case report forms, source documents, and regulatory documents; assesses the maintenance and security of study records, test articles, and study specimens; reviews the informed consent process; and serves as an institutional liaison.
Additional Information:
Preferred Qualifications
SOCRA CCRP certification or ACRP-CP certification
Responsible for monitoring activities to assure compliance. Provides reviews of case report forms, source documents, and regulatory documents; assesses the maintenance and security of study records, test articles, and study specimens; reviews the informed consent process; and serves as an institutional liaison.
Required Education:
High school diploma or GED or equivalent
Recommended Education:
Bachelor's degree in a related field of study.
Required Work Experience:
High School Diploma/GED and 2 years of relevant experience, or 4 years of experience in lieu of a diploma/GED.
Recommended Work Experience:
Required Certifications:
Recommended Certifications:
Description
1. Develop, implement, and maintain a monitoring program and tools for human research.
2. Obtain documents and assure the files are complete.
3. Conduct initial, interim and close-out monitoring visits for all designated studies.
4. Communicate issues and status of monitoring activities, potential findings, and education opportunities.
5. Reviews contracts for required elements.
6. Develop procedures, tools, internal systems trend analyses, quality improvement efforts and monitor its effect.
7. Assist in educational activities/training, coordinate trends in audits, and be a content resource.
8. Assist research project development, drafting forms, and reviewing documents.
9. Other duties as assigned