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Open nowPosted 4 days ago

Research Monitoring Specialist

Arkansas Children's229 open roles

Where
Little Rock
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Your applicationOpen nowResearch Monitoring SpecialistArkansas Children's · Little Rock

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. Arkansas Children's postings stay open a median of 30 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 4 days ago

Arkansas Children's median: 30 days open

The posting

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

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