Senior CNS CRA — Remote, West Coast Travel

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

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site qualification through closeout, ensuring protocol adherence and high data quality. This home-based role supports West Coast sites and travels regionally to manage investigations with sponsors and global teams.

You will lead monitoring, site management, and regulatory compliance, training site staff and driving safety and data accuracy across the trial lifecycle.

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional, traveling Clinical Research Associate.
• Experience monitoring CNS clinical trials.
• Willingness to travel within the region; 8–10 days per month.
• Experience in full-service monitoring is preferred.

Responsibilities

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

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to oversee site qualification through closeout, ensuring protocol adherence and high data quality. This home-based role supports West Coast sites and travels regionally to manage investigations with sponsors and global teams.

You will lead monitoring, site management, and regulatory compliance, training site staff and driving safety and data accuracy across the trial lifecycle.