Hybrid Oncology Clinical Research Coordinator 4

Avispa Technology; Palo Alto (CA); Hybrid; USD 45,000 - 65,000; Full time

Benefits offered by this job

Health benefits

Retirement savings program

Dental & Vision coverage

Job summary

A leading university in Palo Alto, CA is seeking a Clinical Research Coordinator 4 to coordinate oncology treatment studies from start-up through closeout. This hybrid role requires interfacing with participants, sponsors, and regulatory bodies while ensuring data integrity and regulatory compliance.

The position involves coordinating multi-site study activities, managing documentation, and collaborating with finance to monitor study budgets.

Qualifications

• Bachelor's degree required.
• SOCRA or ACRP certification preferred.
• Onsite clinical research experience preferred.
• Experience with EPIC EMR and MS Office.

Responsibilities

• Serve as primary contact with participants, sponsors, and regulatory bodies for study coordination.
• Determine eligibility, obtain consent, and assist with recruitment strategies.
• Collect and manage patient and lab data; maintain study documents and CRFs.
• Ensure protocol compliance; prepare regulatory submissions and IRB renewals.
• Assemble study kits, schedule procedures, monitor budgets, and resolve billing issues.

Skills

Regulatory coordination

Data management

Communication

Education

Bachelor's degree in related field

Tools

EPIC EMR

Microsoft Office

Job description

A leading university in Palo Alto, CA is seeking a Clinical Research Coordinator 4 to coordinate oncology treatment studies from start-up through closeout. This hybrid role requires interfacing with participants, sponsors, and regulatory bodies while ensuring data integrity and regulatory compliance.

The position involves coordinating multi-site study activities, managing documentation, and collaborating with finance to monitor study budgets.