Research Coordinator I- Oncology

WakeMed Health & Hospitals•Raleigh, NC

About The Position

The Research Coordinator I will assist investigators and the research team with the planning and implementation of oncology clinical trials. Duties include subject recruitment and consent, research procedures as appropriate, case report form (CRF) completion, communication and meetings with sponsor representatives, scheduling and assisting with clinical trial monitoring activities, research billing reviews, IRB submissions, and reporting adverse events and protocol deviations.

Requirements

  • High school diploma or equivalent required.

Nice To Haves

  • One year of clinical research experience preferred.

Responsibilities

  • Assist investigators and the research team with planning and implementing clinical trials.
  • Recruit subjects and obtain consent.
  • Perform research procedures as appropriate.
  • Complete case report forms (CRFs).
  • Communicate and meet with sponsor representatives.
  • Schedule and assist with clinical trial monitoring activities.
  • Complete research billing reviews.
  • Complete IRB submissions.
  • Report adverse events and protocol deviations.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service