Senior CNS CRA - Remote (West Coast Travel)

Worldwide Clinical Trials Holdings, Inc.; California; Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) for a home-based role supporting sites across the West Coast. You will monitor studies, qualify sites, initiate monitoring, and ensure regulatory compliance while partnering with sponsors and study teams to drive data quality and patient safety.

The position requires 5+ years as a regional, traveling CRA, experience monitoring CNS trials, and the ability to travel 8–10 days per month.

Qualifications

• Bachelor's degree or Nursing degree required.
• 5+ years as a regional traveling CRA.
• Experience monitoring CNS clinical trials.
• Willingness to travel 8–10 days per month within the region.

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies.
• Identify and assess potential research sites to support successful study execution.
• Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs and COVs.
• Train site personnel on protocol requirements, data collection processes, and safety reporting expectations.
• Monitor site performance and provide ongoing support throughout study maintenance activities.
• Ensure compliance with informed consent requirements, safety reporting obligations and applicable regulatory standards.
• Partner with sites and study teams to drive data quality, participant safety, and overall study success.
• Support site closeout activities and ensure study requirements are completed at the conclusion of the trial.

Skills

Clinical Research

Site Management

Regulatory Knowledge

Travel Flexibility

Monitoring Visits

CNS Trials

Education

Bachelor's Degree

Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) for a home-based role supporting sites across the West Coast. You will monitor studies, qualify sites, initiate monitoring, and ensure regulatory compliance while partnering with sponsors and study teams to drive data quality and patient safety.

The position requires 5+ years as a regional, traveling CRA, experience monitoring CNS trials, and the ability to travel 8–10 days per month.