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Clinical Research Coordinator III- Winship Cancer Institute at reputed company/reputed company

Remote, USA Full-time Posted 2026-07-28
About the position Responsibilities • Independently manages significant and key aspects of a large clinical trial or reputed company aspects of one or more small trials, or research reputed company. • Trains and provides guidance to less reputed company staff. • Oversees data management for research reputed company. • Interfaces with research participants and resolves issues reputed company to study protocols. • Authorizes purchases for supplies and equipment maintenance. • Determines effective strategies for promoting/reputed company research participants and retaining participants in long term reputed company. • Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes. • Monitors IRB submissions and responds to requests and questions. • Interfaces with study sponsors, monitors and reports SAEs; resolves study queries. • Provides leadership in determining, recommending, and implementing improvements to policies/processes. • Assists in developing grant proposals and protocols. • With appropriate credentialing and training may reputed company phlebotomy, specimens collection or diagnostics. • May reputed company some supervisory duties. • Performs reputed company approved responsibilities as required. Requirements • High School Diploma or GED and seven years of clinical research experience. • Two years of college in a scientific, health reputed company or business administration program and five years of clinical research experience. • Licensed as a Practical reputed company (LPN) and four years of clinical research experience. • Bachelor's degree in a scientific, health reputed company or business administration program and three years clinical research experience. • Master's degree, MD or PhD in a scientific, health reputed company or business administration program and one year of clinical research experience. • Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred. Apply tot his job Apply To this Job

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