Senior Clinical Research Associate — Remote Midwest Travel

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

Job summary

Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate to ensure quality study execution across CNS and Rare Disease trials, providing leadership and regulatory oversight while supporting investigators, sponsors, and global teams.

Based in the Midwest United States, you will travel 8–10 days per month to sites, supervise monitoring activities, and drive data quality and patient safety throughout the trial lifecycle.

Qualifications

• Bachelor's Degree or Nursing Degree with 5+ years as a regional traveling CRA
• Experience monitoring CNS and Rare Disease trials
• Willingness to travel within the specified region; 8-10 days per month

Responsibilities

• Manage clinical research activities at investigative sites participating in Worldwide studies
• Coordinate study start-up activities, including regulatory documentation and support of contract and budget processes
• Conduct 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, safety reporting obligations, and regulatory standards
• Partner with sites and study teams to drive data quality and participant safety
• Support site closeout activities and ensure study requirements are completed

Skills

5+ years CRA

Education

Bachelor's or Nursing Degree

Job description

Worldwide Clinical Trials, a global CRO, is seeking a Senior Clinical Research Associate to ensure quality study execution across CNS and Rare Disease trials, providing leadership and regulatory oversight while supporting investigators, sponsors, and global teams.

Based in the Midwest United States, you will travel 8–10 days per month to sites, supervise monitoring activities, and drive data quality and patient safety throughout the trial lifecycle.