[Hiring] Clinical Research Data Coordinator @City of Hope

Role Description

The Clinical Research Data Coordinator will build and maintain data standards for all clinical trials, and assist with study start up including:

• Protocol review
• Case report form and database review
• Dataset specifications
• Data transfer specifications
• Review of data management and handling plans

Additionally, the coordinator will:

• Develop and implement the data correction process
• Handle discrepancy resolution
• Oversee data control activities
• Conduct data validation with source documents

Will support clinical trial studies from preparation through closeout including regulatory submissions by standardizing data management.

• Ensure source documentation and management of clinical study data is in accordance with FDA regulations and ICH/GCP guidelines
• Attend all SIVs and Monitor visits
• Enter data in the CTMS and provide weekly/monthly enrollment reports

Qualifications

• Knowledge of or ability to learn medical/oncology terminology
• Experience using Microsoft Access and Excel or EDC systems (Inform, TrialManager, Medidata, RedCap)
• Minimum of an Associate Degree in life sciences or information systems
• Experience in the health field preferred
• 2-3 years clinical/oncology experience preferred

Requirements

• Prioritizes work based on deadlines
• Seeks clarification on data entry requirements from providers
• Works directly with supervisor and providers to identify data points and answer queries
• Ability to work independently and thrive in a results-oriented environment

Benefits

• City of Hope is an equal opportunity employer
• Pay is based on work experience, qualifications, and work location