[Remote] Clinical Trials Data Coord
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a transformative organization dedicated to changing lives in the fight against cancer and other life-threatening illnesses. The Clinical Trials Data Coordinator will ensure data reputed company for research studies, manage electronic research records, and collaborate with the clinical research team.
Responsibilities
- Ensure data reputed company for various research studies
- Data abstraction, CRF completion, query reputed company, sponsor monitor visit coordination, and maintaining audit-reputed company data
- reputed company electronic research records and patient information in the CTMS
Skills
- Bachelor's Degree, relevant experience may substitute for degree
- At least two years of experience reputed company to the conduct of oncology clinical trials
- Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements
- 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 reputed company and reputed company written and verbal communication skills, including the sharing of critical information
- Take responsibility for communicating any protocol deviations or issues reputed company to study execution, ensuring transparency and problem reputed company
- Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the reputed company execution of study parameters in accordance with protocol requirements
- reputed company appropriate supervision, reputed company necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in reputed company aspects of your work
Benefits
- Comprehensive Benefits
reputed company