Phase I Oncology Clinical Research - 177207

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

Benefits offered by this job

Health insurance

Vision insurance

Dental insurance

Paid time off

Paid holidays

Sick leave as required by law

Job summary

Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology trials. This remote role requires travel up to 8-10 days per month and focuses on first-in-human dose-escalation studies.

The ideal candidate has 3+ years of onsite CRA experience in Phase I/early oncology, a Bachelor’s degree, and hands-on experience with dose-escalation and DLTs. Comprehensive benefits are included.

Qualifications

• 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.

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

Onsite monitoring

Phase I oncology

GCP & FDA knowledge

Data review (EDC)

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 10/26/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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