Oncology CRA II

Piper Companies; United States; Remote; USD 115,000 - 127,000; Full time

Benefits offered by this job

Remote work option

Job summary

Piper Companies is seeking an Oncology CRA II to join a leading clinical research organization within the oncology and pharmaceutical industry. The Oncology CRA II will monitor oncology trials, ensure regulatory compliance, maintain data integrity, and support investigative sites throughout the trial lifecycle.

The role requires travel to sites 8-10 days per month and a strong background in site monitoring, ICH-GCP, and FDA regulations.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• 3+ years of clinical monitoring experience as a CRA with oncology trial work.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes.
• Experience conducting site monitoring visits independently; proficient with EDC and CTMS.

Responsibilities

• Conduct site qualification, initiation, routine monitoring, and closeout visits for oncology trials.
• Ensure compliance with ICH-GCP guidelines, study protocols, sponsor requirements, and applicable regulatory standards.
• Review source data and verify trial data for accuracy, completeness, and consistency.
• Identify, document, and resolve site issues, protocol deviations, and data discrepancies.
• Develop relationships with investigators, study coordinators, and site personnel.
• Support patient recruitment, retention efforts, and study enrollment goals.
• Prepare monitoring reports and maintain trial master file documentation.
• Collaborate with cross-functional clinical operations teams to ensure successful study execution.

Skills

Oncology monitoring

Site monitoring

ICH-GCP

FDA regulations

EDC

CTMS

Data verification

Regulatory compliance

Education

Bachelor's degree in Life Sciences, Nursing, Pharmacy

Tools

EDC systems

CTMS platforms

Job description

Piper Companies is seeking an Oncology CRA II to join a leading clinical research organization within the oncology and pharmaceutical industry. The Oncology CRA II will be responsible for monitoring oncology clinical trials, ensuring regulatory compliance, maintaining data integrity, and supporting investigative sites throughout the clinical trial lifecycle. This opportunity is ideal for a clinical research professional with strong monitoring experience and a background in oncology studies. The Oncology CRA II role requires you to travel to sites 8-10 days per month.

Responsibilities of the Oncology CRA II:

• Conduct site qualification, initiation, routine monitoring, and closeout visits for oncology clinical trials.
• Ensure compliance with ICH-GCP guidelines, study protocols, sponsor requirements, and applicable regulatory standards.
• Review source documentation and verify clinical trial data for accuracy, completeness, and consistency.
• Identify, document, and resolve site issues, protocol deviations, and data discrepancies.
• Develop strong relationships with investigators, study coordinators, and site personnel.
• Support patient recruitment, retention efforts, and study enrollment goals.
• Prepare monitoring reports and maintain trial master file documentation.
• Collaborate with cross-functional clinical operations teams to ensure successful study execution.

Requirements of the Oncology CRA II:

• Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
• 3+ years of clinical monitoring experience as a CRA with oncology trial experience.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes.
• Experience conducting site monitoring visits independently.
• Proficiency with EDC systems, CTMS platforms, and clinical trial documentation.

Compensation for the Oncology CRA II:

• Salary range: $115,000 - $127,000 base salary
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.

Keywords:

Oncology CRA, Clinical Research Associate, CRA II, Oncology Clinical Trials, ICH-GCP, Site Monitoring, Clinical Operations, FDA Regulations, Source Data Verification, SDV, EDC, CTMS, Clinical Monitoring Visits, Oncology Research, Pharmaceutical Industry, Biotechnology, Protocol Compliance, Trial Management, Site Management, Oncology Studies, Investigative Sites, Clinical Research

This job opens for applications on 10/09/2026. Applications for this job will be accepted for at least 30 days from the posting date.

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