Senior Clinical Research Associate

Piper Companies is seeking a Senior Clinical Research Associate (CRA) to support a well-established organization within the clinical research industry for a remote, contract opportunity. The Senior Clinical Research Associate (CRA) will oversee monitoring activities across oncology and general medicine studies, working with a mix of therapeutic areas while supporting sites throughout the region.

Responsibilities of the Senior Clinical Research Associate include:

· Perform on-site and remote monitoring visits to confirm studies are conducted in accordance with GCP, ICH, and applicable regulatory standards.

· Collaborate with investigative sites to support enrollment efforts and adjust recruitment strategies when challenges arise.

· Deliver protocol-related training and serve as a key liaison between study teams and site staff.

· Review site performance for protocol and regulatory compliance, escalating risks or quality concerns as appropriate.

· Monitor overall study progress, including regulatory milestones, enrollment status, data review, and issue resolution.

Qualifications for the Senior Clinical Research Associate include:

· Minimum of 3 years of recent on-site monitoring experience, including oncology trials (solid and/or liquid tumors).

· Experience supporting studies across multiple therapeutic areas, including general medicine.

· Working knowledge of CTMS, EDC platforms, and Microsoft Office tools.

· Strong understanding of GCP, ICH guidelines, and clinical research regulations.

· Bachelor’s degree in life sciences, nursing, or a related discipline (advanced degree preferred).

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 4/1/26. 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.

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