Oncology Clinical Data Coordinator (EDC & QC)

Caris MPI, Inc.; Irving (TX); On-site; USD 64,000 - 72,000; Full time

Benefits offered by this job

Medical, dental & vision insurance

401(k) match and financial planning

Paid time off

Job summary

Caris Life Sciences in Irving, TX seeks a Clinical Data Coordinator to ensure high data integrity for oncology trials across the Caris Precision Oncology Alliance sites. You will abstract data from source documents, enter into EDC forms, resolve data queries, and support QA audits while adhering to GCP, FDA, IRB, and HIPAA standards.

You will collaborate with on-site teams, manage site data timelines, and help maintain study documentation and data quality across protocols and projects.

Qualifications

• Knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Experience handling oncology study data and terminology.
• Proficient in entering data into EDC systems and maintaining data quality.

Responsibilities

• Abstract clinical data from source documents.
• Enter data into study-specific EDC case report forms.
• Clean data and verify accuracy; update EDC after data verification.
• Track site goals and CRF completion; prioritize site cases for analysis.
• Maintain study documentation and perform QC audits of the database.
• Ensure compliance with GCP, FDA, IRB and HIPAA; adhere to SOPs.
• Collaborate with the onsite team to confirm proper consenting and data abstraction.
• Travel to multiple investigative sites if required; communicate with study personnel.

Skills

GCP/ICH knowledge

Oncology data terminology

Clinical data entry

EDC systems

Data integrity

Communication skills

Tools

EDC systems

Job description

Caris Life Sciences in Irving, TX seeks a Clinical Data Coordinator to ensure high data integrity for oncology trials across the Caris Precision Oncology Alliance sites. You will abstract data from source documents, enter into EDC forms, resolve data queries, and support QA audits while adhering to GCP, FDA, IRB, and HIPAA standards.

You will collaborate with on-site teams, manage site data timelines, and help maintain study documentation and data quality across protocols and projects.