Phase I Oncology Clinical Research - 177492

Piper Companies; United States; Remote; USD 110,000 - 140,000; Full time

Job summary

Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology clinical trials. The position is remote and requires travel up to 8-10 days per month.

The ideal candidate has 3+ years of onsite monitoring in Phase I or early-phase oncology and a Bachelor’s degree. The role emphasizes monitoring in compliance with ICH-GCP and FDA regulations, site initiation to close-out visits, and collaboration with sites and internal teams.

Qualifications

• 3+ years of onsite monitoring as a CRA in 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.

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.

Skills

Site monitoring

GCP knowledge

FDA regulations

Oncology

Travel readiness

Education

Bachelor's degree

Tools

EDC systems

Job description

Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology clinical trials within the biotechnology and pharmaceutical industry. The Phase I Oncology Clinical Research Associate role is ideal for a clinical research professional experienced with first-in-human and dose-escalation oncology studies. The Phase I Oncology Clinical Research Associaterole is a remote opportunity and requires you to travel up to 8-10 days per month.

Responsibilities of the Phase I Oncology Clinical Research Associate:

• 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 of the Phase I Oncology Clinical Research Associate:

• 3+ years of onsite monitoring as a CRA with a focus on Phase I or early-phase oncology.
• Bachelors 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 for the Phase I Oncology Clinical Research Associate:

• $110,000 - $140,000 base salary
• Full Comprehensive 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

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

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