Oncology Clinical Data Coordinator

The START Center for Cancer Research; Grand Rapids (MI); On-site; USD 42,000 - 60,000; Full time

Benefits offered by this job

401(k) match

Annual bonus

Paid time off

Medical/dental/vision coverage

Life and disability insurance

Employee Assistance Program

Job summary

The START Center for Cancer Research is seeking a Data Coordinator to collect, enter, transcribe, and transmit clinical data for assigned investigational drug studies at our Grand Rapids site. This role supports oncology trials and requires meticulous data management.

You will review data for completeness, coordinate monitor visits, and ensure timely data entry. A High School Diploma and 2 years of data entry experience are required; CCRP/CCRC credentials are a plus.

Qualifications

• High school diploma or GED required.
• 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 assigned 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, including exit meetings with monitors.
• Identify labs and communicate with Regulatory Affairs for lab certifications.
• Review and utilize study protocols for study activities.
• Assure data entry remains current for all assigned studies.
• Attend meetings for assigned studies (site initiation, monitor exit, close-out, audits).
• Other duties may be assigned at any time.

Skills

Data entry

Medical terminology

Office administration

Computer applications

Education

High School Diploma/GED

Bachelor’s degree

CCRP or CCRC credentials

Tools

MS Office

CRF systems

Job description

The START Center for Cancer Research is seeking a Data Coordinator to collect, enter, transcribe, and transmit clinical data for assigned investigational drug studies at our Grand Rapids site. This role supports oncology trials and requires meticulous data management.

You will review data for completeness, coordinate monitor visits, and ensure timely data entry. A High School Diploma and 2 years of data entry experience are required; CCRP/CCRC credentials are a plus.