Oncology Clinical Data Coordinator

The START Center for Cancer Research; Grand Rapids (MI); On-site; USD 42,000 - 66,000; Full time

Benefits offered by this job

401(k) retirement savings plan with-em

Annual performance bonus

Generous paid time off and paidholid

Medical, dental, and vision coverage

Life and disability insurance

Flexible FSA and HSA plans

Commitment to balance and wellbeing

Collaborative, learning-focused work环境

Job summary

The START Center for Cancer Research in Grand Rapids, MI is seeking a Data Coordinator to collect, transcribe, and transmit clinical data for investigational drug studies. The role focuses on accurate data entry across paper and electronic CRFs, with travel up to 10% for site monitoring and meetings.

Ideal candidates have 2 years of clinical data entry experience, high school diploma or GED, and familiarity with medical terminology. A Bachelor's degree and CCRP/CCRC credentials are preferred.

Qualifications

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

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 for assigned studies, including exit meetings with monitors.
• Identify labs used for assigned studies and communicate with Regulatory Affairs to request lab certifications.
• Review and utilize study protocols as guides for study activities.

Skills

Data entry

Medical terminology

Education

High School Diploma/GED

Bachelor's degree

CCRP/CCRC credentials

Job description

The START Center for Cancer Research in Grand Rapids, MI is seeking a Data Coordinator to collect, transcribe, and transmit clinical data for investigational drug studies. The role focuses on accurate data entry across paper and electronic CRFs, with travel up to 10% for site monitoring and meetings.

Ideal candidates have 2 years of clinical data entry experience, high school diploma or GED, and familiarity with medical terminology. A Bachelor's degree and CCRP/CCRC credentials are preferred.