Clinical Data Coordinator – Oncology Trials

START Research; Pittsburgh (Allegheny County); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

401(k) retirement savings plan with-em

Annual performance bonus

Paid time off and holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA

Collaborative environment and growth

Job summary

The START Center for Cancer Research in Pittsburgh is seeking a Data Coordinator to collect, enter/transcribe, and transmit clinical data for investigational drug studies. This role supports CRFs, data corrections, and data quality across assigned trials.

Ideal candidates have a High School Diploma/GED and at least 2 years of clinical data entry experience, plus strong office administration skills. A Bachelor's degree and CCRP/CCRC credentials are preferred.

Qualifications

• High School Diploma or GED required; 2+ years of clinical data entry experience.
• Familiarity with medical terminology and data accuracy.
• General office administration skills including documentation and data handling.

Responsibilities

• Collect, enter/transcribe, and transmit/submit clinical data for investigational studies.
• Review patient data for completeness and accuracy for assigned studies.
• Coordinate and schedule monitor visits and review data with monitors.
• Identify and communicate lab facilities needs to Regulatory Affairs for certs.
• Ensure data entry remains current and respond to data queries promptly.
• Attend meetings related to assigned studies and support audit preparations.

Skills

Clinical data entry

Office administration

Computer applications

Education

High School Diploma/GED

Bachelor's degree (preferred)

CCRP or CCRC credentials (desirable)

Tools

Microsoft Office Suite

Job description

The START Center for Cancer Research in Pittsburgh is seeking a Data Coordinator to collect, enter/transcribe, and transmit clinical data for investigational drug studies. This role supports CRFs, data corrections, and data quality across assigned trials.

Ideal candidates have a High School Diploma/GED and at least 2 years of clinical data entry experience, plus strong office administration skills. A Bachelor's degree and CCRP/CCRC credentials are preferred.