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

Benefits offered by this job

401(k) retirement savings plan with_em

Annual performance bonus

Paid time off and holidays

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA and HSA plans

Culture of learning and growth

Job summary

The START Center for Cancer Research is hiring a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will work under senior staff to ensure protocol adherence, data accuracy, and patient safety in a fast-paced setting.

Responsibilities include patient screening, consent, data collection, and coordination of forms and training. Strong knowledge of GCP, regulatory requirements, and MS Office is required; experience with trial management software is a plus.

Qualifications

• High School Diploma or GED required.
• Minimum 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, especially Phase 1.
• Strong attention to detail and accurate data collection.
• Working knowledge of GCP and regulatory requirements.
• Proficiency in MS Office and trial management software.

Responsibilities

• Support daily activities of early phase oncology trials under supervision.
• Ensure protocol compliance, regulatory adherence, and patient safety.
• Interact with patients, collect data, and maintain accurate study documentation.
• Screen patients for eligibility and facilitate informed consent processes.
• Coordinate forms, training, and site procedures; monitor study conduct.
• Assist with case report forms, data queries, and SAE reporting with PI.
• Collaborate with sponsors, CROs, and staff to resolve protocol questions.

Skills

Attention to detail

Regulatory knowledge

Data collection

GCP

Communication

Team coordination

Patient interaction

Monitoring

Education

High School Diploma or GED

Oncology trial exposure (preferred)

Tools

MS Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research is hiring a Clinical Research Coordinator to support daily activities of early-phase oncology trials. You will work under senior staff to ensure protocol adherence, data accuracy, and patient safety in a fast-paced setting.

Responsibilities include patient screening, consent, data collection, and coordination of forms and training. Strong knowledge of GCP, regulatory requirements, and MS Office is required; experience with trial management software is a plus.