Clinical Research Coordinator

Job Description

Clinical Research Coordinator to coordinate and perform daily clinical research activities for the Ohio State Universitys 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 inservices 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.

Minimum Education Required

Bachelors degree in biological sciences, health sciences or other health sciences related field or an equivalent combination of education and experience required;

Qualifications

One year experience in a clinical research capacity experience or knowledge in clinical research required; knowledge of medical terminology desired; computer skills required; experience using Microsoft Software applications required.

Research and Scholarship - Clinical Research - Individual Contributor - Specialized - S2 Experienced