Phase I Oncology Clinical Research Coordinator

The START Center for Cancer Research

East Brunswick Township (NJ)

On-site

USD 52,000 - 62,000

Full time

5 days ago
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Benefits offered by this job

401(k) match
Annual bonus
Paid time off
Medical/dental/vision
Life & disability insurance
EAP
Flexible FSA/HSA
Collaborative culture

Job summary

The START Center for Cancer Research is seeking a Clinical Research Coordinator to support early‑phase oncology trials under the guidance of senior staff. The role focuses on accurate data collection, patient interaction, and compliant trial conduct.

You will ensure protocol adherence, regulatory compliance, and timely study activities, coordinating with sponsors and CROs as needed. This is a patient‑facing, detail‑driven position in a fast‑paced setting.

Qualifications

  • High school diploma or GED required.
  • 2 years of clinical research experience supporting interventional studies.
  • Strong oncology trial experience, especially Phase 1.
  • Strong attention to detail and accuracy in data collection and documentation.
  • Ability to manage multiple tasks and meet deadlines in a fast-paced environment.
  • Working knowledge of GCP and regulatory requirements.
  • Proficiency in Microsoft Office and trial management software.

Responsibilities

  • Communicate with Study Sponsors/CROs and staff regarding questions and protocol status.
  • Monitor day-to-day conduct of studies per protocol, SOPs and GCP.
  • Create/revise forms to assure protocol compliance.
  • Maintain files with standardized labeling and filing procedures.
  • Assist with patient screening and eligibility.
  • Facilitate informed consent process ensures proper completion.
  • Identify deviations and coordinate corrective actions with leadership.
  • Assist data coordinator with case report forms and queries.
  • Work with PI to complete and submit Serious Adverse Event reports.
  • Perform protocol-closeout activities with data coordination.

Skills

Attention to detail
Multi-tasking
GCP knowledge
Regulatory compliance

Education

High School Diploma or GED

Tools

Microsoft Office Suite
Clinical trial management software

Job description

The START Center for Cancer Research is seeking a Clinical Research Coordinator to support early‑phase oncology trials under the guidance of senior staff. The role focuses on accurate data collection, patient interaction, and compliant trial conduct.

You will ensure protocol adherence, regulatory compliance, and timely study activities, coordinating with sponsors and CROs as needed. This is a patient‑facing, detail‑driven position in a fast‑paced setting.

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