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This position will require occasional onsite presence, so Ohio residency is required.
Position Summary
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 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.
Job Requirements
Bachelors 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; knowledge of medical terminology desired; computer skills required; experience using Microsoft Software applications required.
Research and Scholarship – Clinical Research – Individual Contributor – Specialized – S2 Experienced
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