Senior CNS CRA — West Coast (Remote Travel)

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

Benefits offered by this job

Competitive benefits package

Equal opportunity employer

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role supporting sites across the West Coast of the United States. You will monitor sites, ensure protocol adherence and regulatory compliance, and collaborate with sponsors and global teams to drive data quality and patient safety.

Your responsibilities include site qualification, study start-up, monitoring visits (PSSVs, SIVs, IMVs, COVs), training site staff, and coordinating regulatory documentation.

Qualifications

• Bachelor’s Degree or a Nursing Degree, along with 5+ years as a regional, traveling Clinical Research Associate.
• Required experience monitoring CNS clinical trials.
• Requires travel within the specified region; 8 – 10 DOS monthly

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

Regional CRA experience

CNS clinical trials monitoring

Travel within region

Full-service monitoring

Regulatory knowledge

Education

Bachelor’s or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a home-based role supporting sites across the West Coast of the United States. You will monitor sites, ensure protocol adherence and regulatory compliance, and collaborate with sponsors and global teams to drive data quality and patient safety.

Your responsibilities include site qualification, study start-up, monitoring visits (PSSVs, SIVs, IMVs, COVs), training site staff, and coordinating regulatory documentation.