Clinical Research Coordinator - Comprehensive Cancer Center

The Ohio State University

1d • Remote

About The Position

Clinical Research Coordinator to coordinate and perform daily clinical research activities for the Ohio State University’s Comprehensive Cancer Center (OSUCCC) Clinical Trials Processing Laboratory; functioning as an integral part of a team working with multi-disciplinary programs; coordinates correlative specimen study start-up; reviews clinical trial protocols for feasibility and accuracy of correlative specimen needs; communicates with Clinical Trials Office Protocol implementation team on questions and revisions; reviews and edits laboratory manuals and study calendars; represents the CTPL at site study implementation and initiation meetings; communicates with sponsors as well as internal and external laboratories where samples are sent for analysis; create study specific educational materials for in-services for clinical research staff; ensures all tasks are completed to allow studies to open in a timely manner; reviews amendments to existing protocols and communicates with sponsors as well as internal and external customers to ensure changes to correlative specimen needs are updated accurately.

Requirements

• Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education and experience required.
• One year experience in a clinical research capacity experience or knowledge in clinical research required
• computer skills required
• experience using Microsoft Software applications required

Nice To Haves

• knowledge of medical terminology desired

Responsibilities

• coordinates correlative specimen study start-up
• reviews clinical trial protocols for feasibility and accuracy of correlative specimen needs
• communicates with Clinical Trials Office Protocol implementation team on questions and revisions
• reviews and edits laboratory manuals and study calendars
• represents the CTPL at site study implementation and initiation meetings
• communicates with sponsors as well as internal and external laboratories where samples are sent for analysis
• create study specific educational materials for in-services for clinical research staff
• ensures all tasks are completed to allow studies to open in a timely manner
• reviews amendments to existing protocols and communicates with sponsors as well as internal and external customers to ensure changes to correlative specimen needs are updated accurately.

Benefits

• Eligible Ohio State employees receive comprehensive benefits packages, including medical, dental and vision insurance, tuition assistance for employees and their dependents, and state or alternative retirement options with competitive employer contributions.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level