Oncology Clinical Data Coordinator

The START Center for Cancer Research

Myrtle Beach (SC)

On-site

USD 40,000 - 60,000

Full time

4 days ago
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Benefits offered by this job

401(k) retirement savings plan with up
Annual performance bonus
Paid time off and paid holidays
Medical, dental, and vision coverage
Life and disability insurance
Employee Assistance Program (EAP)
Flexible FSA and HSA plans
Diversity and collaboration culture

Job summary

The START Center for Cancer Research, located at Myrtle Beach, SC, is seeking a Data Coordinator to collect, transcribe, and submit clinical data for investigational drug studies. You will ensure data accuracy, coordinate monitor visits, and manage CRFs from multiple sites.

Required: 2 years of clinical data entry, high school diploma, and strong office skills; CCRP/CCRC credentials and medical terminology familiarity are preferred. Travel up to 10% may be required.

Qualifications

  • High School Diploma or GED required.
  • 2 years of clinical data entry experience.
  • General office administration skills including computer applications.
  • Bachelor’s degree preferred; CCRP/CCRC credentials encouraged.
  • Familiarity with medical terminology preferred.

Responsibilities

  • Collect, enter/transcribe, and transmit/submit clinical data for investigational studies.
  • Receive and request patient records/data as needed to complete CRFs.
  • Review patient data for completeness and accuracy.
  • Coordinate and schedule monitor visits and site initiation/close-out meetings.
  • Identify lab facilities and communicate needs for lab certifications.

Skills

Data entry
CRF completion
Medical terminology
Office administration

Education

High School Diploma/GED
Bachelor’s degree
CCRP or CCRC credentials

Tools

CRF software

Job description

The START Center for Cancer Research, located at Myrtle Beach, SC, is seeking a Data Coordinator to collect, transcribe, and submit clinical data for investigational drug studies. You will ensure data accuracy, coordinate monitor visits, and manage CRFs from multiple sites.

Required: 2 years of clinical data entry, high school diploma, and strong office skills; CCRP/CCRC credentials and medical terminology familiarity are preferred. Travel up to 10% may be required.

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