Senior Clinical Research Associate – Psychiatry

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

📋 Description

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

• Evaluate and identify suitable research sites.

• Manage study initiation activities, which include regulatory documentation, contract negotiations, and budget processes.

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

• Provide training to site personnel regarding protocol specifications, data collection methods, and safety reporting procedures.

• Monitor site performance and assist with ongoing study activities.

• Ensure compliance with informed consent, safety reporting, and regulatory standards.

• Collaborate with sites and study teams to enhance data quality, ensure participant safety, and achieve study objectives.

• Assist in site closeout procedures and fulfill study obligations.

⛳️ Requirements

• A Bachelor's Degree or a Nursing Degree is required.

• A minimum of 5 years' experience as a regional, traveling Clinical Research Associate.

• Proven experience in monitoring CNS and Alzheimer's clinical trials.

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

• Preferred experience in full-service monitoring.

• In-depth understanding of clinical trial processes, site management, and regulatory obligations.

• Candidates must reside within the central region of the United States.

🏝️ Benefits

• A competitive benefits package tailored to the location.

• Transparent compensation and commitment to pay equity.