- Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations.
- Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information.
- Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution.
- Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements.
- Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work.
- Bachelor's Degree, relevant experience may substitute for degree.
- At least two years of experience related to the conduct of oncology clinical trials.
- Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.
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Clinical Trials Data Coordinator - Duarte, United States - City of Hope
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Description
Clinical Trials Data Coordinator - Remote
Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses.
City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix.
Our dedicated and compassionate employees are driven by a common mission:To deliver the cures of tomorrow to the people who need them today.
This full-time remote position entails ensuring data integrity for various research studies. Responsibilities include data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintaining audit-ready data. You will also oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research.
As a successful candidate, you will:
Your qualifications should include:
To learn more about our Comprehensive Benefits, please CLICK HERE.