Clinical Trials Content Specialist

Job Summary

A company is looking for an OnCore Content Specialist - Clinical Trials.

Key Responsibilities

• Analyze and process newly submitted studies and their documentation for calendar builds
• Build and maintain study calendars in the OnCore Clinical Trials Management System (CTMS) according to best practices
• Collaborate with related departments and assist in the development of internal SOPs for data entry and system use

Required Qualifications

• Bachelor's Degree or equivalent combination of education and experience
• Two years of experience in an academic medical center, research administration, or related fields
• Working knowledge of oncology clinical trials and related documentation
• Experience reading protocols and understanding their requirements
• Experience building clinical trial calendars in OnCore CTMS