Senior CRA – CNS/Rare Disease | Remote Midwest

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

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to support CNS and rare disease studies from a home-based role across the Midwest United States. You will travel regionally (approximately 8–10 days per month) to monitor sites, drive data quality, ensure patient safety, and maintain regulatory compliance.

You will collaborate with sponsors, study teams, and investigative sites, providing leadership and site management throughout the trial lifecycle.

Qualifications

• Bachelor's Degree or a Nursing Degree, plus 5+ years as a regional, traveling Clinical Research Associate.
• Experience monitoring CNS and Rare Disease clinical trials.
• Travel within the specified region; 8-10 days per month.
• Experience in full-service monitoring is preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirements.

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

Travel monitoring

Site management

CNS/Rare Disease monitoring

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to support CNS and rare disease studies from a home-based role across the Midwest United States. You will travel regionally (approximately 8–10 days per month) to monitor sites, drive data quality, ensure patient safety, and maintain regulatory compliance.

You will collaborate with sponsors, study teams, and investigative sites, providing leadership and site management throughout the trial lifecycle.