Sr. Contract Clinical Research Associate

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

Benefits offered by this job

Health benefits

Vision benefits

Dental benefits

Paid time off

Paid holidays

Sick leave

Job summary

Piper Companies is seeking a Sr. Contract Clinical Research Associate (Oncology) to support oncology trials. This remote role requires travel of 8-10 days per month across U.S. regions and is a contract opportunity.

The candidate should have 5+ years of CRA experience, 3+ years in oncology monitoring, and a solid understanding of ICH-GCP and FDA regulations. Travel flexibility is essential for oncology trials.

Qualifications

• 5+ years of CRA experience in pharma, biotech, or CRO environments.
• 3+ years of strong oncology clinical trial monitoring experience.
• Solid understanding of ICH-GCP and FDA regulations.

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 monitoring

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.

Keywords: senior clinical research associate, sr cra, oncology cra, oncology clinical trials, contract cra, clinical monitoring, ich-gcp, cro, pharmaceutical, biotechnology, remote cra, clinical research associate, cra, oncology

This job opens for applications on 11/6/2026. Applications for this job will be accepted for at least 30 days from the posting date.