Remote CNS Senior CRA – West Coast, 8–10 Days/Month

Worldwide Clinical Trials; Arizona; Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior CRA to ensure studies meet quality, patient safety, and regulatory standards. You’ll lead monitoring across the trial lifecycle, support site qualification, and collaborate with study teams and sponsors to drive reliable data.

This home-based role supports West Coast sites, with travel about 8–10 days per month. You’ll train site personnel, manage regulatory documentation, and ensure protocol adherence while maintaining strong relationships with

Qualifications

• Bachelor's or Nursing degree with 5+ years as a traveling CRA.
• Experience monitoring CNS clinical trials.
• Willing to travel within West Coast region (8–10 DOS monthly).
• Experience in full-service monitoring preferred.
• Strong knowledge of trial processes, site management, and regulatory requirements.

Responsibilities

• Manage clinical research activities at investigative sites.
• Identify and assess potential research sites.
• Coordinate start-up activities and regulatory documentation.
• Conduct monitoring visits: PSSV, SIV, IMV, COV.
• Train site personnel on protocol and data collection.
• Monitor site performance and provide ongoing support.
• Ensure informed consent, safety reporting, and regulatory compliance.
• Collaborate with sites and sponsors to drive data quality.
• Support site closeout activities.

Skills

Regional travel experience

CNS clinical trials monitoring

Full-service monitoring (preferred)

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior CRA to ensure studies meet quality, patient safety, and regulatory standards. You’ll lead monitoring across the trial lifecycle, support site qualification, and collaborate with study teams and sponsors to drive reliable data.

This home-based role supports West Coast sites, with travel about 8–10 days per month. You’ll train site personnel, manage regulatory documentation, and ensure protocol adherence while maintaining strong relationships with