Senior CRA - Oncology - 173755 - 174661

ZP Group; United States; Remote; USD 90,000 - 140,000; Full time

Benefits offered by this job

Medical, Dental, Vision

Retirement plans

Remote flexibility

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support late-phase oncology trials. The role focuses on hands-on site monitoring, trial execution, and a relationship-driven approach within a dynamic biotech team.

The Senior CRA will oversee Phase II–III oncology studies, conduct on-site visits, and ensure adherence to ICH-GCP and SOPs. Remote flexibility is offered with regional travel requirements, suitable for experienced oncology CRAs.

Qualifications

• Experience in oncology trials and senior CRA responsibilities.
• Independent monitoring and full lifecycle trial oversight.
• Strong client-facing experience with biotech sponsors.

Responsibilities

• Oversee Phase II–III oncology studies independently, ensuring adherence to ICH-GCP guidelines and study protocols.
• Perform on-site monitoring visits (approx. 8 days monthly) including initiation, interim monitoring and close-out.
• Conduct source data verification and CRF assessments to maintain audit-ready data quality.
• Build partnerships with investigative sites to drive enrollment and ensure protocol compliance.
• Identify site risks, escalate issues, and keep milestones on track.

Skills

Oncology monitoring

Site monitoring

ICH-GCP

Job description

Piper Companies is actively seeking a Senior Clinical Research Associate (CRA) to join a growing team supporting late-phase oncology trials within the biotech industry. The Senior Clinical Research Associate (CRA) position is ideal for professionals who thrive in a high-velocity environment and bring a hands-on, relationship-driven approach to clinical site monitoring and trial execution.

Responsibilities of the Senior Clinical Research Associate (CRA):

• Oversee Phase II–III oncology studies independently, ensuring adherence to ICH-GCP guidelines, study protocols, and internal SOPs
• Perform on-site monitoring visits (approximately 8 days monthly), including site initiation, interim monitoring, and close-out activities
• Conduct source data verification/review and case report form assessments to maintain audit-ready data quality
• Build strong partnerships with investigative sites to drive enrollment, ensure protocol compliance, and resolve operational challenges
• Proactively identify site risks, elevate issues, and ensure milestones and study deliverables remain on track

Qualifications of the Senior Clinical Research Associate (CRA):

• Proven experience as a Senior CRA with a focus on oncology clinical trials (required)
• Demonstrated expertise in independent monitoring and full lifecycle trial oversightPrior experience working directly with biotech sponsors in a client-facing capacity
• Ability to manage multiple clinical sites and competing priorities with limited supervision
• Hands-on oncology site monitoring experience

Compensation for the Senior Clinical Research Associate (CRA) includes:

• Salary range: Based on Experience
• Comprehensive benefits package including medical, dental, vision, and retirement plans
• Remote flexibility with regional travel requirements

This job opens for applications on 10/02/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: Senior Clinical Research Associate, CRA, Oncology, Clinical Trials, Monitoring, Biotech, ICH-GCP, Remote, Phase II, Phase III, Site Monitoring

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