Senior CRA - Remote in Central US for CNS & Rare Disease

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

Job summary

Worldwide Clinical Trials seeks a Senior Clinical Research Associate to lead monitoring and site management across CNS and rare disease studies. This home-based role supports Central US sites, travels regionally about 8-10 days per month, and partners with sponsors and study teams to ensure protocol adherence and high data quality.

You will guide site teams, perform a range of monitoring visits, and drive regulatory compliance from start-up through closeout, contributing to safe participant care

Qualifications

• Bachelor's Degree or a Nursing Degree, along with 5+ years as a regional, traveling Clinical Research Associate.
• Required experience monitoring CNS and Rare Disease clinical trials.
• Requires travel within the specified region; 8-10 DOS monthly
• 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

CNS trials

Rare disease trials

Travel readiness

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials seeks a Senior Clinical Research Associate to lead monitoring and site management across CNS and rare disease studies. This home-based role supports Central US sites, travels regionally about 8-10 days per month, and partners with sponsors and study teams to ensure protocol adherence and high data quality.

You will guide site teams, perform a range of monitoring visits, and drive regulatory compliance from start-up through closeout, contributing to safe participant care