Senior CRA - CNS Trials, Home-Based with Regional Travel

Worldwide Clinical Trials; Minneota (MN); Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure high-quality study conduct, patient safety, and regulatory compliance across Midwest sites. This home-based role supports investigators, sponsors, and study teams, guiding site activities and data quality.

Travel is required, approximately 8–10 days per month, with regional travel to support site visits. Candidates should have a bachelor's or nursing degree and 5+ years as a traveling CRA, with CNS monitoring

Qualifications

• Bachelor's Degree or Nursing Degree with 5+ years as a regional traveling CRA.
• Experience monitoring CNS clinical trials.
• Willingness to travel within the specified region; ~8–10 days per month.
• Experience in full-service monitoring 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 qualify potential study sites to support trial execution.
• Coordinate study start-up activities, including regulatory documentation and support of contract and budget processes.
• Conduct all types of monitoring visits: PSSVs, SIVs, IMVs, 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, safety reporting, and 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 end of the trial.

Skills

CNS clinical trial monitoring

Site management

Regulatory knowledge

Travel readiness

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to ensure high-quality study conduct, patient safety, and regulatory compliance across Midwest sites. This home-based role supports investigators, sponsors, and study teams, guiding site activities and data quality.

Travel is required, approximately 8–10 days per month, with regional travel to support site visits. Candidates should have a bachelor's or nursing degree and 5+ years as a traveling CRA, with CNS monitoring