Oncology Clinical Data Coordinator

START Research; Grand Rapids (MI); Hybrid; USD 42,000 - 70,000; Full time

Benefits offered by this job

401(k) retirement savings plan with 2%

Performance bonus eligibility

Generous paid time off & holidays

Medical/dental/vision coverage

Job summary

START Research in Grand Rapids, MI is seeking a Data Coordinator to collect, enter, and transmit clinical data for investigational drug studies. The role emphasizes accuracy of CRFs and timely data entry across paper and electronic formats.

You will work with the study team to obtain records, review data quality, and schedule monitor visits, contributing to QA and regulatory readiness in a collaborative environment.

Qualifications

• 2 years of clinical data entry experience.
• Knowledge of general office administration skills, including computer applications.
• Familiarity with medical terminology and clinical data concepts.

Responsibilities

• Collect, enter/transcribe, and transmit/submit clinical data in paper and/or electronic CRFs.
• 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, including exit meetings with monitors.
• Identify lab facilities used for studies and inform Regulatory Affairs for certifications.
• Review protocols to guide study activities and ensure data entry remains current.
• Attend meetings related to assigned studies (site initiation, monitor exit, audits).
• Other duties may be assigned at any time.

Skills

Clinical data entry

Data coordination

Medical terminology

Team coordination

Education

High School Diploma/GED

Bachelor’s degree (preferred)

Tools

CRFs

EDC systems

Job description

START Research in Grand Rapids, MI is seeking a Data Coordinator to collect, enter, and transmit clinical data for investigational drug studies. The role emphasizes accuracy of CRFs and timely data entry across paper and electronic formats.

You will work with the study team to obtain records, review data quality, and schedule monitor visits, contributing to QA and regulatory readiness in a collaborative environment.