Hybrid Clinical Data Coordinator — Oncology & EDC

Caris Life Sciences; Phoenix (AZ); Hybrid; USD 64,000 - 80,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

HSA

Paid time off

401k match

Long-term disability

Employee assistance

Tuition assistance

Job summary

Caris Life Sciences seeks a Clinical Data Coordinator I to support data entry for oncology protocols at Caris Precision Oncology Alliance sites. You will abstract data from source documents, enter into EDC CRFs, and maintain data quality with QC checks while adhering to GCP, IRB, and HIPAA standards.

The role requires 3–5 years in data collection within a GCP/regulatory environment, familiarity with EDC systems, and strong medical terminology. Hybrid role with some in-office work.

Qualifications

• 3-5 years of experience in data collection within a GCP/clinical research regulatory environment.
• Knowledgeable in GCPs, ICH, and CFRs.
• Clinical study experience in Oncology.
• Strong medical terminology understanding.
• Experience with EDC systems.
• Proficient in Microsoft Office (Word, Excel, Outlook).

Responsibilities

• Abstract clinical data from subject source documentation.
• Enter clinical data into study-specific EDC case report forms.
• Perform data cleaning and verification, resolve data queries.
• Track site goals and CRF completion; prioritize site cases.
• Maintain study documentation; perform QC audits of the database.
• Ensure compliance with GCP, IRB, HIPAA; coordinate with onsite team.

Job description

Caris Life Sciences seeks a Clinical Data Coordinator I to support data entry for oncology protocols at Caris Precision Oncology Alliance sites. You will abstract data from source documents, enter into EDC CRFs, and maintain data quality with QC checks while adhering to GCP, IRB, and HIPAA standards.

The role requires 3–5 years in data collection within a GCP/regulatory environment, familiarity with EDC systems, and strong medical terminology. Hybrid role with some in-office work.