Clinical Research Associate

Piper Companies is seeking a Clinical Research Associate (CRA) with experience in Oncology clinical trials to join a reputable clinical research organization. This is a full-time/permanent opportunity. Some travel is required (regionally, about 8-10 days out of the month). Candidates must be located in CST or PST in one of the following states: WY, CO, KS, WI, IN, OH, MN, MO, IL, MI, KY, AR, CA, OR, WA, NV, UT, AZ.

Responsibilities of the Senior Clinical Research Associate (CRA):

• Perform site selection, initiation, monitoring, and close-out visits in accordance with GCP and ICH guidelines.
• Create and monitor recruitment plans with sites to ensure project goals are achieved.
• Deliver protocol training to sites and maintain ongoing communication to manage expectations and address any issues.
• Review site practices for adherence to protocols and regulatory requirements, escalating any quality concerns as needed.
• Manage regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution, and support start-up phases as required.

Qualifications of the Senior Clinical Research Associate (CRA):

• Minimum of 2 years of clinical monitoring experience; preference for CRO experience
• At least 1 year of experience in Oncology
• Familiarity with FDA, ICH GCP, and local regulations

Compensation for the Senior Clinical Research Associate:

• Salary Range: $110,000-$120,000 based on experience
• Comprehensive Benefits including Medical, Dental, Vision, 401k, PTO, Sick Leave (if required by law), & Holidays

This job opens for applications on 4/15/2025. Applications for this job will be accepted for at least 30 days from the posting date.  

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Keywords: CRA, Clinical Research Associate, Oncology Clinical Trials, site monitoring, patient records, protocol adherence, regulatory compliance, recruitment plans, study training, trial status reports, data management, SOPs, client audits, FDA regulations, ICH GCP, communication skills, organizational skills, CRO experience, therapeutic area, quality assurance, study progress management, Trial Master File, Investigator’s Site File, informed consent, adverse event reporting, clinical trial management systems (CTMS), electronic data capture (EDC), site initiation visits, monitoring visits, close-out visits, regulatory submissions, data query resolution, clinical study reports, site audits, investigator meetings, protocol deviations, risk management, site feasibility assessments.