Contract Clinical Research Associate

New Opportunity- Part- time contract CRA (USA Contract)

I have an exciting part-time Clinical Research Associate role, on site based in Anaheim California!

This role is a 12 month part time contract, 4-8 hours per month on site, perfect for a monitor with experience in Gastrointestinal studies and spare time in the month to take on and support an extra project.

Experience in Oncology is also favored however not required.

Responsibilities:

• Site Management: Oversee the conduct of clinical trials at site, ensuring adherence to protocol, GCP, and regulatory requirements.
• Monitoring: Conduct interim monitoring, and close-out visits to evaluate the progress of trials, verify data, and ensure patient safety.
• Documentation: Maintain accurate and timely documentation of site activities, including monitoring reports, regulatory documents, and correspondence.
• Communication: Serve as the primary point of contact between site and the sponsor/CRO, ensuring effective communication and resolution of issues.
• Quality Assurance: Perform routine site audits and coordinate inspections by regulatory authorities, ensuring compliance with study protocols and regulations.
• Training: Provide training and support to investigational site staff on protocol requirements, data collection, and study procedures.
• Data Management: Assist in the review and validation of clinical trial data to ensure accuracy, completeness, and consistency.
• Project Management: Contribute to project planning, timeline management, and resource allocation to meet study milestones and deliverables.