Note: The job is a remote job and is open to candidates in USA. City of Hope is a healthcare and research organization focused on fighting cancer, diabetes, and other life-threatening illnesses. The Clinical Trials Data Coordinator ensures data integrity for research studies through data abstraction, CRF completion, query resolution, sponsor monitor visit coordination, and maintenance of audit-ready data. The role also oversees electronic research records and patient information in the CTMS while supporting clinical research compliance.
Responsibilities
- 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
- 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
- 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
Benefits
- Full-time remote position
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