Senior Clinical Research Associate – Psychiatry

This is a fully remote position, open to applicants in Kansas.

📋 Description

• Oversee clinical research operations at investigative sites involved in global clinical studies.

• Identify and evaluate potential research sites.

• Organize study initiation activities, including regulatory documentation, contracts, and budgeting processes.

• Conduct Pre-study Site Visits (PSSVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Close-Out Visits (COVs).

• Educate site staff on protocol requirements, data collection methods, and safety reporting procedures.

• Monitor site performance and assist with ongoing study maintenance tasks.

• Ensure informed consent, safety reporting, and adherence to regulatory standards.

• Collaborate with sites and study teams to enhance data quality, participant safety, and overall study success.

• Assist with site closeout processes and ensure completion of study obligations.

⛳️ Requirements

• Bachelor’s Degree or a Nursing Degree.

• Over 5 years of experience as a regional, traveling Clinical Research Associate.

• Background in monitoring CNS and psychiatric clinical trials.

• Willingness to travel within the designated region; approximately 8–10 days of travel per month.

• Preference for candidates with experience in full-service monitoring.

• Strong understanding of clinical trial processes, site management, and regulatory obligations.

• Candidates must be located within the Central United States region.

🏝️ Benefits

• Competitive benefits package based on location.

• Transparent compensation structure and commitment to pay equity.