About The Position

Regulatory Assistant to provide support to assure research protocols are in compliance with university, state and federal regulations across research groups managed by the Clinical Trials Office (CTO).

Requirements

  • Bachelor's degree, preferably in biological sciences, health sciences, or life sciences or equivalent combination of education and experience required.
  • Experience in a clinical research capacity desired.
  • Computer skills required with knowledge of database software applications desired.

Responsibilities

  • Assists with regulatory functions in support of clinical research activity.
  • Assists in preparation of protocol submissions to Institutional Review Boards (IRBs) and provides updates on submission status.
  • Assists in preparation of other required regulatory documents.
  • Distributes approved documents.
  • Relays information to clinical research staff.
  • Assists with data entry including collecting, entering and maintaining data and documents in the OnCore electronic database.
  • Assists with monitoring visits.
  • Assists with regulatory issues.
  • Creates and maintains regulatory files.

Benefits

  • Comprehensive benefits packages, including medical, dental and vision insurance.
  • Tuition assistance for employees and their dependents.
  • State or alternative retirement options with competitive employer contributions.
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