Jobs · Information Technology · Arkansas

Clinical Research Professional I - Bilingual Preferred (Spanish/English)

Arkansas Children's · Little Rock, AR · 2 wk ago
Information TechnologyFull-time

Summary

The Clinical Research Professional I coordinates selected specific aspects of clinical research studies. This role 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.

Requirements

  • High School Diploma/GED, or 2 years of experience in lieu of a diploma/GED.
  • Bachelor's degree in a related field of study preferred.
  • Required certifications: Certified Clinical Research Coordinator (CCRC) from the Association of Clinical Research Professionals, or Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates.

Qualifications

  • High school diploma or GED.
  • 2 years of experience in lieu of a diploma/GED.

Skills

  • Ability to recruit and screen patients for enrollment eligibility and participation in research projects.
  • Ability to obtain consent for participation in accordance with all government regulations and internal policies/procedures.
  • Ability to prepare flowcharts, study specific source documents, and collect/record subject data on case report forms.
  • Ability to create databases and perform date entry into the database.
  • Ability to serve as a research resource to subjects, families, and other healthcare providers regarding the needs of the study and subjects' family, preserving patient/subject privacy and maintaining confidentiality of subject information.
  • Ability to promote knowledge of current professional practice and research standards, laws, and regulations that affect human subjects research.
  • Ability to facilitate and improve collaboration with other departments to facilitate research across the continuum.
  • Ability to coordinate/collect requested data for sponsor review during site visits.
  • Ability to assist study monitors in chart and case report form review.
  • Ability to maintain files and study documentation according to institutional and regulatory standards.

Benefits

  • Tobacco-free workplace policy.
  • Flu vaccines are required.

Pay

N/A

Schedule

Please see job description for details.

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