Clinical Trial Data Coordinator I

Moffitt; Tampa, Northern (FL, KY); Híbrido; USD 29.000 - 43.000; Jornada completa

Descripción de la vacante

The Research Data Coordinator I at Moffitt Cancer Center in Tampa, FL, supports data management across multiple clinical studies by extracting data from medical records, lab reports, and patient questionnaires according to study protocols.

Under supervision, you will enter data into study databases, resolve data discrepancies, prepare for audits, and collaborate with study coordinators and monitors to ensure data quality and protocol adherence.

Formación

• Abstract information from data collection tools or subject's medical record and enters required protocol data into the study designated data control system.
• Ensures data is entered/reported in a timely manner keeping with clinical trial agreements and SOPs.
• Applies an understanding of medical terminology related to anatomy, physiology, oncology, pathology, radiology and cancer treatment modalities.
• Maintains electronic and paper files necessary for data abstraction and follow-up functions in an organized fashion.

Responsabilidades

• Abstract and enter data from medical records into the study designated data control system.
• Identify and resolve data discrepancies with investigators and study team.
• Prepare data for monitoring/audit reviews and draft responses as needed.
• Collaborate with study coordinators to document enrollment, treatment, and follow-up data.
• Maintain organized electronic and paper filing for data abstraction and follow-up.

Conocimientos

Data management

CRF review

Medical terminology

Data entry

SOP adherence

Team collaboration

Educación

High School Diploma / GED

AA/AS degree acceptable

Descripción del empleo

The Research Data Coordinator I at Moffitt Cancer Center in Tampa, FL, supports data management across multiple clinical studies by extracting data from medical records, lab reports, and patient questionnaires according to study protocols.

Under supervision, you will enter data into study databases, resolve data discrepancies, prepare for audits, and collaborate with study coordinators and monitors to ensure data quality and protocol adherence.