Senior CRA — Remote Midwest Travel for CNS Trials

Worldwide Clinical Trials; Wisconsin; Remote; USD 85,000 - 120,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to lead site monitoring and management across CNS trials. This home-based role supports investigative sites throughout the Midwest, with travel approximately 8-10 days per month.

You will ensure protocol adherence, safety reporting, and regulatory compliance while guiding study teams and sponsors. The ideal candidate has 5+ years of regional, traveling CRA experience, strong knowledge of clinical trial processes, and

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; Experience in full-service monitoring preferred.
• Strong knowledge of clinical trial processes, site management, and regulatory requirement.

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: Pre-Site Selection Visits (PSSVs), Study Initiation Visits (SIVs), Interim Monitoring Visits (IMVs) and Closeout Visits (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

Clinical monitoring

Site management

Regulatory compliance

Team collaboration

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CRA) to lead site monitoring and management across CNS trials. This home-based role supports investigative sites throughout the Midwest, with travel approximately 8-10 days per month.

You will ensure protocol adherence, safety reporting, and regulatory compliance while guiding study teams and sponsors. The ideal candidate has 5+ years of regional, traveling CRA experience, strong knowledge of clinical trial processes, and