Clinical Research Professional I

Arkansas Children's HospitalLittle Rock, AR
Onsite

About The Position

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 or GED or equivalent
  • 2 years of experience in lieu of a diploma/GED

Nice To Haves

  • Bachelor's degree in a related field of study
  • Certified Clinical Research Coordinator (CCRC) - Association of Clinical Research Professionals
  • Certified Clinical Research Professional (CCRP) - Society of Clinical Research Associates

Responsibilities

  • Recruits and screens patients for enrollment eligibility and participation in research projects.
  • Obtains consent for participation in accordance with all government regulations and internal policies/procedures.
  • Prepares flowcharts, study specific source documents, and collects/records subject data on case report forms.
  • Creates databases and performs date entry into the database.
  • Serves as a research resource to subjects, families, and other healthcare providers regarding the needs of study and subjects family preserving patient/subject privacy and maintaining confidentiality of subject information.
  • Promotes knowledge of current professional practice and research standards, laws and regulations that affect human subjects research.
  • Facilitates and improves collaboration with other departments to facilitate research across the continuum.
  • Coordinates/collects requested data for sponsor review during site visits.
  • Assists study monitor(s) in chart and case report form review.
  • Maintains files and study documentation according to institutional and regulatory standards.
  • Performs other duties as assigned.
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