Oncology Clinical Research Coordinator – Early-Phase Trials

The START Center for Cancer Research

Grand Rapids (MI)

On-site

USD 55,000 - 75,000

Full time

11 days ago

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Benefits offered by this job

401(k) plan with company match
Annual performance bonus
Paid time off & holidays
Medical, dental, vision coverage
Life and disability insurance
Employee Assistance Program

Job summary

The START Center for Cancer Research in Grand Rapids is seeking a Clinical Research Coordinator to support the daily activities of early-phase oncology trials. Under supervision, you will ensure protocol adherence, data collection, and patient safety in accordance with GCP.

You will screen patients, coordinate visits, manage regulatory documents, and train staff on procedures. Our team offers competitive compensation and comprehensive benefits.

Qualifications

  • High School Diploma or GED required.
  • At least 2 years of clinical research experience.
  • Strong attention to detail and accuracy in data collection.

Responsibilities

  • Communicate with sponsors, CROs, and staff regarding protocol status.
  • Monitor day-to-day conduct to ensure protocol, SOP, and GCP compliance.
  • Maintain and review trial documents and labeling for protocol compliance.
  • Train staff on protocol amendments and trial procedures.
  • Assist with patient screening and eligibility determination.
  • Support informed consent processes and adverse event reporting.
  • Collaborate with data coordinators on CRF completion and queries.

Skills

Attention to detail
Data collection
Regulatory compliance
GCP knowledge
Microsoft Office

Education

High school diploma or GED

Tools

Clinical trial management software
Microsoft Office

Job description

The START Center for Cancer Research in Grand Rapids is seeking a Clinical Research Coordinator to support the daily activities of early-phase oncology trials. Under supervision, you will ensure protocol adherence, data collection, and patient safety in accordance with GCP.

You will screen patients, coordinate visits, manage regulatory documents, and train staff on procedures. Our team offers competitive compensation and comprehensive benefits.

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