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

📋 Description

• Oversee clinical research operations at investigative sites engaged in Worldwide clinical trials.

• Identify and evaluate potential research locations.

• Organize study initiation activities, encompassing regulatory documentation and the contract and budget processes.

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

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

• Monitor site performance and assist with study maintenance tasks.

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

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

• Assist in site closure and fulfillment of study obligations.

⛳️ Requirements

• Bachelor's Degree or a Nursing Degree.

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

• Required experience in monitoring CNS and Rare Disease clinical trials.

• Willingness to travel within the designated region; 8–10 days on-site monthly.

• Preferred experience in full-service monitoring.

• In-depth knowledge of clinical trial processes, site management, and regulatory requirements.

• Candidates must be residents of the Midwest region of the United States.

• Capability to travel to investigative sites for approximately 8–10 days each month.

🏝️ Benefits

• Competitive benefits package tailored to location.

• An inclusive and equitable work environment.

• Equal employment opportunities for all candidates.

• Clear compensation structure and pay equity.