Phase I Oncology Clinical Research Associate

Responsibilities

• Monitor Phase I and first-in-human oncology trials in compliance with ICH-GCP and FDA regulations.
• Conduct site initiation, monitoring, and close-out visits.
• Ensure subject safety, data quality, and protocol adherence.
• Review source documents, EDC data, and safety reports.
• Collaborate with sites and internal clinical teams to resolve issues.

Requirements

• 3+ years of onsite monitoring as a CRA with a focus on Phase I or early-phase oncology.
• Bachelor's Degree is Required.
• Hands-on experience with dose-escalation and DLTs.
• Strong knowledge of GCP, FDA regulations, and monitoring best practices.
• Experience with oncology indications and EDC systems.
• Ability to travel to research sites as required.

Compensation

$110,000 - $140,000 base salary

Benefits

• Health
• Vision
• Dental
• PTO
• Paid Holiday and Sick Leave if Required by Law

Keywords

Phase One Oncology CRA, Clinical Research Associate, Phase I Oncology, First-in-Human Trials, Dose Escalation, Oncology Clinical Research, GCP, FDA Regulations, Clinical Monitoring, Biotechnology, Pharmaceutical

Application Information

This job opens for applications on 7/10/2026. Applications for this job will be accepted for at least 30 days from the posting date.