This is a fully remote position, open to applicants in Michigan, +1 more state.

📋 Description

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

• Evaluate and identify potential research sites to ensure effective study implementation.

• Coordinate the initiation of studies, including the gathering of regulatory documents and assisting with contract and budget processes.

• Conduct Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits.

• Educate site staff on protocol specifications, data collection methods, and safety reporting responsibilities.

• Assess site performance and offer continuous support throughout the study maintenance phase.

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

• Collaborate with sites and study teams to enhance data integrity, participant safety, and overall study effectiveness.

• Assist with site closeout tasks and confirm that all study obligations are fulfilled at the trial's end.

⛳️ Requirements

• Bachelor's Degree or a Nursing Degree.

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

• Experience in monitoring CNS clinical trials is essential.

• Travel within the designated region is required; approximately 8–10 days of travel per month.

• Previous experience in full-service monitoring is preferred.

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

🏝️ Benefits

• Competitive salary and performance-based bonuses.

• Comprehensive health and wellness benefits package.

• Opportunities for professional development and continuing education.

• Flexible working arrangements to support work-life balance.