Senior CRA - CNS & Rare Disease | Remote Midwest

Worldwide Clinical Trials

Texas

Remote

USD 97,000 - 193,000

Full time

6 days ago
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Job summary

Worldwide Clinical Trials is seeking a Senior CRA to ensure high-quality site monitoring and regulatory compliance across Midwest sites. You will lead monitoring activities from site qualification through closeout, partnering with study teams and sponsors to deliver reliable data.

This home-based role requires 5+ years as a traveling CRA, experience in CNS and Rare Disease trials, and regular travel within the region.

Qualifications

  • Bachelor's or Nursing degree required.
  • 5+ years as regional, traveling CRA.
  • Experience monitoring CNS and Rare Disease trials.
  • Willingness to travel regionally; 8–10 DOS monthly.
  • Experience in full-service monitoring preferred.

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 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

Bachelor/Nursing Degree
5+ years regional CRA
CNS monitoring
Rare Disease monitoring
Travel 8-10 DOS monthly
Full-service monitoring

Education

Bachelor's Degree
Nursing Degree

Job description

Worldwide Clinical Trials is seeking a Senior CRA to ensure high-quality site monitoring and regulatory compliance across Midwest sites. You will lead monitoring activities from site qualification through closeout, partnering with study teams and sponsors to deliver reliable data.

This home-based role requires 5+ years as a traveling CRA, experience in CNS and Rare Disease trials, and regular travel within the region.

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