Senior CRA, CNS & Rare Disease — Remote Midwest

Worldwide Clinical Trials Holdings, Inc.; Texas; Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is a global CRO dedicated to delivering high-quality clinical research. We seek a Senior CRA who will partner with investigative sites, study teams, and sponsors to ensure protocol adherence, data integrity, and patient safety across trials.

This home-based Midwest role requires 5+ years as a regional travelling CRA, CNS and Rare Disease monitoring experience, and travel about 8–10 days per month.

Qualifications

• Bachelor's Degree or Nursing Degree required.
• 5+ years as a regional traveling Clinical Research Associate.
• Experience monitoring CNS and Rare Disease trials.

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 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

Site monitoring

Regulatory knowledge

Education

Bachelor's degree

Nursing degree

Job description

Worldwide Clinical Trials is a global CRO dedicated to delivering high-quality clinical research. We seek a Senior CRA who will partner with investigative sites, study teams, and sponsors to ensure protocol adherence, data integrity, and patient safety across trials.

This home-based Midwest role requires 5+ years as a regional travelling CRA, CNS and Rare Disease monitoring experience, and travel about 8–10 days per month.