Regulatory Assistant - Clinical Trials Office - Remote

Overview

The Regulatory Assistant provides essential support to ensure compliance with research protocols within the Clinical Trials Office, facilitating the regulatory aspects of clinical research.

In Short

• Assist with regulatory functions for clinical research.
• Prepare protocol submissions to Institutional Review Boards (IRBs).
• Manage updates on submission statuses.
• Distribute approved regulatory documents.
• Relay information to clinical research staff.
• Perform data entry and maintain records in the OnCore database.
• Assist with monitoring visits and regulatory issues.
• Create and maintain regulatory files.
• Work in a remote environment.
• Collaborate with various research groups.

Requirements

• Bachelor's degree in biological, health, or life sciences preferred.
• Experience in a clinical research capacity is desired.
• Strong computer skills required.
• Knowledge of database software applications is a plus.
• Ability to work independently and as part of a team.
• Excellent communication skills.
• Detail-oriented with strong organizational skills.

Benefits

• Comprehensive medical, dental, and vision insurance.
• Tuition assistance for employees and their dependents.
• State or alternative retirement options with competitive employer contributions.
• Supportive work environment focused on excellence.
• Opportunity to contribute to impactful cancer research.