Clinical Research Support Specialist

Job Summary

A company is looking for a Clinical Research Support Specialist to provide administrative and operational support within the Office of Clinical Trials.

Key Responsibilities

• Review clinical trial submissions for completeness and facilitate the review process
• Translate protocol schedules into OnCore and maintain tracking systems
• Monitor IRB submissions and manage the clinical research invoicing mailbox

Required Qualifications

• Bachelor's Degree in Finance, Business Administration, Healthcare, or related field
• At least one year of experience using OnCore
• Minimum two years of administrative experience in a medical or healthcare setting
• Familiarity with clinical trial protocols and basic medical terminology
• Strong computer skills, including proficiency in Microsoft applications