Note: The job is a remote job and is open to candidates in USA. City of Hope is a national healthcare system focused on developing cures and treating cancer, diabetes, and other life-threatening illnesses. The Clinical Trials Data Coordinator ensures data integrity for research studies by managing data abstraction, case report forms, queries, sponsor monitor visits, electronic research records, and patient information in the CTMS.
Responsibilities
- 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
- 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
Skills
- * 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
Benefits
- Full-time remote position
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