Clinical Research Associate (CRA) - 174335

ZP Group; United States; Remote; USD 155,000 - 175,000; Full time

Benefits offered by this job

Medical, dental, vision

401(k)

PTO

Job summary

Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The CRA role is ideal for an experienced monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials.

This role is fully remote for candidates with occasional travel.

Qualifications

• 3+ years as a CRA monitoring interventional trials.
• Experience onsite monitoring for oncology studies and GCP.
• Ability to travel occasionally to investigative sites.
• Knowledge of ICH-GCP and FDA regulations.

Responsibilities

• Oversee oncology trial sites to ensure protocol compliance and patient safety.
• Conduct site qualification, initiation, monitoring and close-out visits for oncology trials.
• Review source data, CRFs, and regulatory documents for accuracy.
• Prepare monitoring visit reports and maintain trial documentation.
• Collaborate with Clinical Operations, Data Management, and Project Management.
• Provide ongoing training and support to investigative sites.

Skills

Oncology trials

GCP compliance

FDA regulations

Remote monitoring

Site management

Travel flexibility

Communication skills

Data integrity

Job description

Piper Companies is seeking a Clinical Research Associate (CRA) to support oncology-focused clinical trials for a leading organization within the life sciences and pharmaceutical research industry. The Clinical Research Associate (CRA) role is ideal for an experienced monitor with a strong background in oncology studies, site management, and ensuring regulatory and protocol compliance across multi-site trials. This role is fully remote for candidates with occasional travel required.

Responsibilities of the Clinical Research Associate:

• Oversee and manage oncology clinical trial sites to ensure protocol compliance, data integrity, patient safety, and adherence to GCP, and SOPs.
• Conduct site qualification, initiation, interim monitoring, and close-out visits for oncology clinical trials.
• Ensure clinical trial activities are conducted in compliance with ICH-GCP, FDA regulations, and study protocols.
• Review and verify source data, case report forms (CRFs), and regulatory documentation for accuracy and completeness.
• Identify, document, and follow up on site issues, protocol deviations, and corrective action plans.
• Serve as the primary point of contact for investigative sites, providing ongoing training and support.
• Collaborate with cross-functional teams including Clinical Operations, Data Management, and Project Management.
• Prepare detailed monitoring visit reports and maintain accurate trial documentation.

Qualifications of the Clinical Research Associate:

• 3+ years of experience as a Clinical Research Associate monitoring interventional clinical trials.
• Hands‑on experience performing onsite monitoring for oncology studies, ensuring GCP compliance and inspection readiness.
• Direct oncology trial monitoring experience is required.
• Strong knowledge of ICH-GCP guidelines, FDA regulations, and clinical research best practices.
• Experience conducting remote and on‑site monitoring visits independently.
• Excellent organizational, communication, and problem‑solving skills.
• Ability to travel occasionally to investigative sites as required.

Compensation for the Clinical Research Associate includes:

• Salary range: $155,000 - $175,000 depending on experience
• Comprehensive benefits package including medical, dental, vision, 401(k), and PTO
• Fully remote work environment with occasional travel

This job opens for applications on 9/14/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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