Oncology Clinical Data Coordinator | EDC & GCP

Caris Life Sciences

United States

Remote

USD 64,000 - 72,000

Full time

12 days ago
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Health Savings Account
Flexible Spending Account
Paid time off
401k match
Long-term disability (LTD)
Short-term disability (STD)
Employee Assistance Program
Pet Insurance
Legal Assistance
Tuition Assistance

Job summary

Caris Life Sciences is seeking a Clinical Data Coordinator to perform data entry for cancer research protocols across the Caris Precision Oncology Alliance sites. This role ensures data integrity and accuracy in CRF data collection and manages entry into EDC systems, coordinating with on-site teams.

The position requires 3–5 years of data collection experience in a GCP environment, knowledge of GCP/ICH guidelines and CFR, and strong Microsoft Excel/Office skills.

Qualifications

  • 3–5 years of data collection experience in a GCP/clinical research regulatory environment.
  • Knowledge of GCPs, ICH guidelines, and CFR.
  • Clinical oncology data experience.
  • Strong medical terminology and data abstraction skills.

Responsibilities

  • Abstract clinical data from subject source documentation.
  • Enter clinical data into the study specific EDC case report forms.
  • Clean the clinical data to verify accuracy.
  • Update the EDC following verification of subject data, including resolution of data queries.
  • Track site goals and case report form completion.
  • Prioritize site cases for analysis.
  • Maintain study specific documentation.
  • Perform QC audits of the clinical database.
  • Work with GCP guidelines and site procedures.

Skills

Clinical data entry
EDC systems
GCP/ICH compliance
Data quality assurance

Tools

Microsoft Word
Microsoft Excel
Microsoft Outlook
EDC platforms

Job description

Caris Life Sciences is seeking a Clinical Data Coordinator to perform data entry for cancer research protocols across the Caris Precision Oncology Alliance sites. This role ensures data integrity and accuracy in CRF data collection and manages entry into EDC systems, coordinating with on-site teams.

The position requires 3–5 years of data collection experience in a GCP environment, knowledge of GCP/ICH guidelines and CFR, and strong Microsoft Excel/Office skills.

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