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

📋 Description

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

• Identify and evaluate potential research locations.

• Coordinate the initiation of studies, which includes managing regulatory documentation and the contract and budget 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 specifications, data collection procedures, and safety reporting measures.

• Track site performance and offer continuous support for study maintenance.

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

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

• Assist with site closeout and fulfill completion of study obligations.

• Travel to investigative sites approximately 8–10 days each month.

⛳️ Requirements

• Bachelor’s Degree or a Nursing Degree.

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

• Proven track record in monitoring CNS and psychiatric clinical trials.

• Willingness to travel within the designated region; 8–10 days of travel monthly required.

• Experience in comprehensive monitoring is preferred.

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

• Candidates should be located within the Central United States territory.

🏝️ Benefits

• Comprehensive benefits package based on location.

• Commitment to an inclusive and equitable workplace.

• Open and transparent compensation with an emphasis on pay equity.