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