CRA II - 176419

Piper Companies; United States; Remote; USD 105,000 - 125,000; Full time

Benefits offered by this job

Health insurance

Paid time off

Dental plan

Vision plan

Travel reimbursement

Job summary

Piper Companies is seeking a Clinical Research Associate II (CRA II) to support oncology trials across Phase I–III. This fully remote role requires regional travel to investigative sites as needed within the United States, offering comprehensive benefits and a strong focus on data quality and regulatory compliance.

The ideal candidate has 3+ years of independent oncology monitoring experience, a life sciences degree, and solid knowledge of ICH-GCP and FDA regulations.

Qualifications

• Bachelor-level degree in life sciences or nursing is required.
• 3+ years of independent oncology monitoring experience.
• Strong knowledge of ICH-GCP and FDA regulations.

Responsibilities

• Conduct routine site monitoring visits for oncology trials.
• Evaluate site compliance with study protocols and regulations.
• Review source documents and ensure data accuracy.
• Collaborate with investigators and cross-functional teams to drive enrollment.
• Prepare monitoring reports and maintain trial documentation.

Skills

Oncology monitoring

Site coordination

Regulatory knowledge

Education

Bachelor's degree in Life Sciences, Nursing, or related field

Job description

Piper Companies is seeking a Clinical Research Associate II (CRA II) to support a growing client in the biotechnology and oncology research industry in the United States. The Clinical Research Associate II (CRA II) role is fully remote with regional travel required to investigative sites as needed. The Clinical Research Associate II (CRA II) role is ideal for a clinical research professional with strong oncology monitoring experience and a proven track record of supporting Phase I-III clinical trials.

Responsibilities of the Clinical Research Associate II (CRA II) include:

• Conduct routine site monitoring visits, including site initiation, interim monitoring, and closeout activities for oncology clinical trials.
• Evaluate site compliance with study protocols, ICH-GCP guidelines, and applicable regulatory requirements.
• Review source documentation and verify clinical data accuracy to ensure high-quality study execution.
• Partner with investigators, study coordinators, and cross-functional teams to proactively resolve site issues and drive enrollment goals.
• Prepare detailed monitoring reports and maintain study documentation throughout the clinical trial lifecycle.

Requirements of the Clinical Research Associate II (CRA II) include:

• Bachelor's degree in Life Sciences, Nursing, or a related scientific field.
• 3+ years of independent monitoring experience as a Clinical Research Associate with a focus on oncology studies.
• Strong knowledge of ICH-GCP, FDA regulations, and clinical trial monitoring best practices.
• Experience supporting Phase I, II, and/or III oncology clinical trials, including site management responsibilities.
• Ability to travel up to 30-50% regionally as required.

Compensation for the Clinical Research Associate II (CRA II) include:

• $105,000 - $125,000 annually
• Full Comprehensive Benefits: Health, Vision, Dental, PTO, Paid Holiday and Sick Leave if Required by Law.
• Fully remote work environment with travel reimbursement.
• This job opens for applications on 10/16/2026. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research associate, CRA II, oncology, clinical trials, monitoring, GCP, FDA, biotech, pharmaceutical, remote, site monitoring, Phase I, Phase II, Phase III, oncology research

#LI-BM4

#LI-REMOTE