Sr. Contract Clinical Research Associate - 175760

ZP Group; United States; Remote; USD 76,000 - 90,000; Part time

Job summary

Piper Companies seeks a Sr. Contract Clinical Research Associate (Oncology) to monitor oncology trials across the U.S. in a remote, contract role requiring travel 8–10 days per month. The ideal candidate has 5+ years of CRA experience and 3+ years in oncology, with strong ICH-GCP knowledge and FDA regulations.

Responsibilities include site initiation, monitoring, and close-out visits, data verification, and timely reporting, while ensuring compliance and trial documentation across multiple sites.

Qualifications

• 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.

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

Oncology monitoring

CRA experience

ICH-GCP knowledge

FDA regulations

Site management

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 10/2/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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