Clinical Research Associate — Travel‑Heavy, Multi‑Site Trials

Ameri-partners; California (MO); Remote; USD 90,000 - 130,000; Full time

Job summary

Ameri Partners is seeking experienced Clinical Research Associates to support a large clinical trial program across multiple U.S. states.

The CRA will manage assigned investigative sites from qualification and initiation through monitoring and closeout, ensuring protocol compliance, data quality, and accurate study documentation. Responsibilities include conducting site visits, ensuring ICH-GCP and FDA compliance, reviewing source documents, and tracking recruitment and milestones.

Qualifications

• Minimum of 5 years of clinical monitoring experience in pharmaceutical, biotechnology, or CRO environments.
• Bachelor’s degree in a scientific, healthcare-related, or relevant field.
• Strong knowledge of clinical trial operations, ICH-GCP, and FDA requirements.
• Experience with CTMS, eTMF, and eCRF platforms.
• Strong communication, organizational, and site management skills.
• Willingness and ability to travel up to 70%.
• CNS clinical trial experience preferred.

Responsibilities

• Conduct site qualification, initiation, interim monitoring, and closeout visits.
• Monitor compliance with study protocols, ICH-GCP, FDA regulations, and sponsor procedures.
• Review source documents, clinical trial data, and essential study records.
• Prepare monitoring reports and follow up on findings and corrective actions.
• Identify and elevate protocol deviations, compliance concerns, and site-performance issues.
• Track recruitment, enrollment, and study milestones.
• Support site staff training and collaborate with Clinical Operations, Data Management, and vendors.
• Manage multiple sites and priorities independently.

Skills

Clinical monitoring

Project management

Communication skills

Travel readiness

Education

Bachelor's degree in science/healthcare

Tools

CTMS

eTMF

eCRF

Job description

Ameri Partners is seeking experienced Clinical Research Associates to support a large clinical trial program across multiple U.S. states.

The CRA will manage assigned investigative sites from qualification and initiation through monitoring and closeout, ensuring protocol compliance, data quality, and accurate study documentation. Responsibilities include conducting site visits, ensuring ICH-GCP and FDA compliance, reviewing source documents, and tracking recruitment and milestones.