About The Position

The Quality Control Clinical Trials team reviews study visits and data collection for accuracy, completeness, and compliance related to oncology clinical trial protocols, department policy, and procedures. The team partners closely with leaders, nurses, data coordinators, and project managers to ensure consistent regulatory compliance and research excellence.

Requirements

  • Graduate of an Accredited School of Nursing, RN required
  • Current applicable state nursing license required
  • CPR certification required
  • Minimum of 3 years clinical trials experience with a pharmaceutical company, Contract Research Organization (CRO), research center or equivalent required

Nice To Haves

  • BSN preferred
  • Oncology experience strongly preferred

Responsibilities

  • Competently fulfills the job responsibilities of the Oncology Research Coordinator, and:
  • Assists Principal Investigator and team in evaluating feasibility of research studies.
  • Develops study budget in collaboration with team.
  • Coordinates documentation for regulatory requirements.
  • Coordinates trial-related activity of patients on protocols.

Benefits

  • Paid Time Off programs
  • medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service