Sr. Contract Clinical Research Associate - 177497

Piper Companies; United States; Remote; USD 76,000 - 90,000; Full time

Benefits offered by this job

Health benefits

PTO

Paid holidays

Sick leave

Job summary

Piper Companies is seeking a Sr. Contract Clinical Research Associate (Oncology) to support oncology trials with the pharma/biotech industry. This senior CRA role is remote and requires travel across multiple U.S. regions, approximately 8–10 days per month, and is a contract opportunity.

The role emphasizes oncology monitoring experience, adherence to ICH-GCP, and the ability to manage sites independently while ensuring high-quality trial conduct and regulatory compliance.

Qualifications

• 5+ years of CRA experience in pharma/biotech/CRO settings.
• 3+ years of oncology monitoring experience.
• Solid understanding of ICH-GCP and FDA regulations.
• Ability to independently manage multiple sites.
• Willingness to travel 8–10 days per month across U.S. time zones.

Responsibilities

• Conduct site initiation, monitoring, and close-out visits for oncology studies.
• Ensure compliance with protocols, ICH-GCP, SOPs, and regulatory requirements.
• Verify source data, CRFs, and EDC entries for accuracy and completeness.
• Identify and document protocol deviations and safety issues.
• Prepare timely monitoring reports and maintain trial documentation.

Skills

CRA experience (oncology)

Oncology monitoring

ICH-GCP knowledge

Regulatory compliance

Travel readiness

Job description

Piper Companies is seeking a Sr. Contract Clinical Research Associate (Oncology) to support oncology clinical trials within the pharmaceutical and biotechnology industry. The Sr. Contract Clinical Research Associate (Oncology) role is ideal for an experienced CRA with strong oncology monitoring experience and the ability to travel across multiple U.S. regions. The Sr. Contract Clinical Research Associate (Oncology) role is a remote opportunity that requires you to travel 8-10 days per month for onsite monitoring and is a contract opportunity.

Responsibilities of the Sr. Contract Clinical Research Associate (Oncology):

• Conduct site initiation, monitoring, and close-out visits for oncology studies.
• Ensure compliance with protocols, ICH-GCP, SOPs, and regulatory requirements.
• Verify source data, CRFs, and EDC entries for accuracy and completeness.
• Identify and document protocol deviations and safety issues.
• Prepare timely monitoring reports and maintain trial documentation.

Requirements of the Sr. Contract Clinical Research Associate (Oncology):

• 5+ years of CRA experience within pharmaceutical, biotechnology, or CRO settings.
• 3+ years of strong oncology clinical trial monitoring experience.
• Solid understanding of ICH-GCP and FDA regulations.
• Ability to independently manage multiple sites.
• Willingness to travel 8–10 days per month across PST, CST, and MST.

Compensation for the Sr. Contract Clinical Research Associate (Oncology):

• $55.00 - $65.00 per hour (Depending on Experience)
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

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.