Senior CRA - Psychiatry | Remote + Central US Travel

Worldwide; Central (LA); Hybrid; USD 97,000 - 193,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CNS/psychiatric) to oversee monitoring and site management for clinical studies. This home-based role covers sites across the Central United States with travel about 8–10 days per month, collaborating with global teams to ensure protocol adherence and patient safety.

Requirements include a Bachelor's or Nursing degree and at least 5 years as a traveling CRA, with experience in CNS/psychiatric trials.

Qualifications

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

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

CNS and psychiatric trial monitoring

Clinical trial monitoring

Site management oversight

Education

Bachelor's or Nursing degree

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CNS/psychiatric) to oversee monitoring and site management for clinical studies. This home-based role covers sites across the Central United States with travel about 8–10 days per month, collaborating with global teams to ensure protocol adherence and patient safety.

Requirements include a Bachelor's or Nursing degree and at least 5 years as a traveling CRA, with experience in CNS/psychiatric trials.