Senior Clinical Research Associate

Piper Companies; United States; Remote; USD 155,000 - 175,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

Paid leave

Job summary

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support oncology trials for a well-established organization. This 6-month remote contract offers potential extensions and full-service monitoring across Phase II and III studies.

The role requires 2+ years of oncology monitoring, autonomous site management, and willingness to travel regionally. You will oversee site performance, ensure GCP/ICH compliance, and prepare monitoring documentation while collaborating with biotech

Qualifications

• Minimum of 2+ years of oncology monitoring experience with expectations of ~3 years independent monitoring.
• Hands-on experience supporting Phase II and Phase III trials in a full-service biotech setting.
• Autonomous work style, able to be sole CRA on a study with minimal oversight.
• Willingness to travel regionally, reside within one hour of a major airport, with onsite visits as required.
• Bachelor's degree not required for senior-level consideration if equivalent experience exists.

Responsibilities

• Manage site monitoring activities for Phase II/III oncology trials, with 8-10 onsite days per month.
• Serve as primary clinical contact for assigned sites and build long-term relationships.
• Ensure study conduct aligns with protocol, GCP, ICH, and regulatory standards.
• Oversee site performance, data quality, and issue resolution, mitigating risks.
• Prepare monitoring documents and follow-up communications in a timely manner.

Skills

Oncology monitoring

Independent monitoring

Site management

Travel readiness

CTMS usage

Tools

CTMS

EDC

Job description

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support oncology clinical trials for a well-established organization within the clinical research industry. This Senior Clinical Research Associate (CRA) role is a 6-month remote contract (with extensions), full-service position.

Responsibilities of the Senior Clinical Research Associate include:

• Independently manage site monitoring activities for Phase II and III oncology trials, including a combination of onsite and remote visits averaging 8-10 onsite days per month.
• Serve as the primary clinical contact for assigned sites, building strong, long-term relationships and providing consistent support and guidance.
• Ensure study conduct aligns with protocol requirements, GCP, ICH guidelines, and applicable regulatory standards.
• Oversee site performance, data quality, and issue resolution while proactively identifying and mitigating risks.
• Prepare accurate and timely monitoring documentation, including visit reports and follow-up communications.

Qualifications for the Senior Clinical Research Associate include:

• Minimum of 2+ years of oncology monitoring experience with current expectations of approximately 3 years of independent monitoring.
• Hands-on experience supporting Phase II and Phase III clinical trials, ideally within a full-service model working with biotechnology clients.
• Ability to operate autonomously, including serving as the sole CRA on a study and managing site relationships with minimal oversight.
• Willingness and ability to travel regionally, reside within one hour of a major airport, and maintain required onsite visit expectations.
• Bachelor's degree not required for senior-level consideration if equivalent clinical research experience can be demonstrated.

Compensation for the Senior Clinical Research Associate:

• Salary: $155,000-$175,000/year (USD)

• Benefits: Medical, Dental, Vision, 401(k), and applicable paid leave

This job opens for applications on 10/30/26. Applications for this job will be accepted for at least 30 days from the posting date.

Keywords: clinical research, clinical trials, CRA, oncology, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, patient recruitment, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas.