Senior CRA - Remote Midwest Travel 8–10 days/mo

Worldwide Clinical Trials; Lansing (MI); Remote; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate for a home-based role covering the Midwest, United States. You will monitor sites, lead regulatory and start-up activities, and drive data quality and patient safety across trials.

You will travel regionally, approximately 8–10 days per month, with full-service monitoring and collaboration with global teams. The position emphasizes regulatory compliance and site leadership.

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional traveling CRA.
• Experience monitoring CNS trials.
• Willingness to travel 8–10 days per month.
• Strong knowledge of 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

Clinical Research Experience

CNS Trials Knowledge

Regional Travel

Regulatory Knowledge

Full-service Monitoring

Education

Bachelor's Degree or Nursing Degree

Job description

Worldwide Clinical Trials is hiring a Senior Clinical Research Associate for a home-based role covering the Midwest, United States. You will monitor sites, lead regulatory and start-up activities, and drive data quality and patient safety across trials.

You will travel regionally, approximately 8–10 days per month, with full-service monitoring and collaboration with global teams. The position emphasizes regulatory compliance and site leadership.