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Compensation

Full Description

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