Ohio Licensed Regulatory Compliance Officer

A company is looking for a Regulatory Compliance Officer for the Clinical Trials Office.

Key Responsibilities

Collaborates with investigators to ensure regulatory safeguards in study development

Conducts reviews of protocols and informed consent forms prior to IRB submission

Acts as the main contact for regulatory agencies and monitors compliance with regulations

Required Qualifications

Bachelor's Degree in biological sciences, health sciences, social sciences, or a related field

One year of experience in a research or administrative role related to research projects

Knowledge of research regulations, guidelines, and compliance issues

Experience in developing informed consent documents and regulatory submissions is desired

Familiarity with IRB and federal or industry sponsor processes is preferred