Remote Clinical Data Coordinator - Oncology Trials

START Center for Cancer Research; Los Angeles (CA); On-site; USD 34,440 - 48,216; Full time

Benefits offered by this job

401(k) retirement savings plan with-em

Performance bonus eligibility

Generous paid time off and holidays

Comprehensive medical, dental, and vis

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA plans

Collaborative and inclusive workplace

Job summary

START Center for Cancer Research in Los Angeles, CA is seeking a Data Coordinator to collect, transcribe, and transmit clinical data for investigational drug studies. The role supports site-based data capture and CRF completion across oncologic trials.

The ideal candidate has 2 years of clinical data entry experience and familiarity with medical terminology. This is an on-site, standard M-F role with competitive compensation and benefits.

Qualifications

• 2 years of clinical data entry experience.
• Knowledge of general office administration skills and computer applications.

Responsibilities

• Collect, enter/transcribe, and transmit/submit clinical data for investigational drug studies.
• Receive and request patient records/data from the study team as required to complete CRFs.
• Review patient data for completeness and accuracy for assigned studies.
• Coordinate and schedule monitor visits for assigned studies.
• Identify labs and communicate with Regulatory Affairs to obtain lab certifications.
• Review protocols as guides for study activities.
• Ensure data entry remains current and attend required meetings.

Skills

Clinical data entry

Office administration

Medical terminology

Education

Bachelor’s degree

High School Diploma/GED

CCRP or CCRC credentials

Job description

START Center for Cancer Research in Los Angeles, CA is seeking a Data Coordinator to collect, transcribe, and transmit clinical data for investigational drug studies. The role supports site-based data capture and CRF completion across oncologic trials.

The ideal candidate has 2 years of clinical data entry experience and familiarity with medical terminology. This is an on-site, standard M-F role with competitive compensation and benefits.