Oncology Clinical Research Associate

Piper Companies is seeking an Oncology Clinical Research Associate (CRA) to join a global leader in advanced analytics, technology solutions, and clinical research services supporting the life sciences and healthcare sectors. This is a full-time opportunity focused on ensuring clinical study sites operate effectively and remain compliant with regulatory and protocol requirements.

Responsibilities of the Oncology Clinical Research Associate (CRA):

·      Perform site selection, site initiation, routine monitoring, and close-out visits while ensuring compliance with Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.

·      Partner with investigative sites to create, implement, and monitor patient recruitment strategies that align with study timelines and project objectives.

·      Deliver protocol-specific training and maintain ongoing communication with site personnel to ensure expectations are clear and challenges are addressed proactively.

·      Assess site performance and processes to ensure adherence to study protocols, identifying and escalating quality or compliance concerns when necessary.

Requirements of the Oncology Clinical Research Associate (CRA):

·      Minimum 3+ years of on-site monitoring experience within Oncology clinical trials.

·      Strong knowledge of GCP and ICH regulations, along with demonstrated expertise in oncology clinical trial protocols.

·      Bachelor’s degree in a scientific, healthcare-related, or equivalent discipline preferred.

Compensation & Benefits

·      Salary Range: $110,000 - $130,000 

·      Comprehensive Benefits: Medical, Dental, Vision, 401(k), Paid Time Off, Sick Leave (as required by law), and Paid Holidays

Keywords: Oncology CRA, Clinical Research Associate, Oncology Monitoring, GCP, ICH, Clinical Trials.

This position opened for applications on July 31, 2026. Applications will be accepted for a minimum of 30 days from the posting date.

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