Oncology Early-Phase Trials Coordinator

The START Center for Cancer Research; East Brunswick Township (NJ); On-site; USD 52,000 - 62,000; Full time

Benefits offered by this job

401(k) match

Annual bonus

PTO and holidays

Medical/dental/vision coverage

Life and disability insurance

EAP

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 integrity, and patient safety.

Responsibilities include patient screening, informed consent, data entry, and coordinating with sponsors/CROs. The role follows standard GCP practices and offers a strong growth path in a dedicated oncology research network.

Qualifications

• Two years of clinical research experience in interventional studies.
• Experience with oncology trials, especially Phase 1.
• Strong data collection and documentation accuracy.
• Familiarity with GCP and regulatory requirements.
• Proficiency in MS Office and trial mgmt software.

Responsibilities

• Coordinate daily activities of early phase oncology trials under senior staff.
• Monitor protocol compliance and patient safety in trials.
• Assist with forms, labeling, and document filing.
• Screen patients and determine eligibility for studies.
• Support informed consent processes and data queries.
• Collaborate with investigators to report Serious Adverse Events.
• Assist with protocol closeouts and data coordination.

Skills

Clinical research experience

Oncology trials

Data collection

Attention to detail

Multitasking

GCP knowledge

Microsoft Office

Trial management software

Education

High School Diploma or GED

Tools

Microsoft 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 integrity, and patient safety.

Responsibilities include patient screening, informed consent, data entry, and coordinating with sponsors/CROs. The role follows standard GCP practices and offers a strong growth path in a dedicated oncology research network.