Senior Clinical Research Coordinator - DoD - Relocation Assistance

Benefits

Qualifications

• •Minimum 5-10 years of experience as Clinical Research Coordinator
• •Active Public Trust or Secret Clearance
• •Minimum of 2 years of clinical site monitoring experience in a clinical research environment

Responsibilities

• •Provide research, regulatory, and administrative support for IRB and IACUC-approved protocols, ensuring compliance with federal and local guidelines
• •Serve as a liaison between research teams, PIs, and regulatory authorities
• •Coordinate study enrollment, subject screening, data collection, participant follow-up, and investigational product accountability per protocol requirements
• •Maintain accurate study records, prepare regulatory reports, and support audits, inspections, and research training initiatives
• •Utilize standard office and clinical information systems (e.g., Word, Excel, CHCS-I, AHLTA) to manage study data and documentation
• •Collaborate with PIs and research staff on study development, funding applications, participant education, and protocol close-out activities, while ensuring HIPAA compliance and patient confidentiality
• •Ensure clinical trial participant safety and data integrity through site visits, source data verification (SDV), and protocol compliance
• •4 more items(s)