Clinical Monitoring

  • Dedicated Team Oversight

    Through our dedicated Clinical Monitoring department, we employ a selective process for CRA recruitment, providing support for each CRA via direct line management, initial and ongoing training  and education, quality oversight from our Clinical Operation Managers, and continued career development, reflecting our commitment to excellence and employee growth.

  • Tailored Sponsor Care

    Vanguard CRAs are dedicated to one Sponsor, allowing them to focus their efforts on understanding the intricate details of the protocol and disease indication, fostering strong partnerships and ensuring protocol compliance, risk mitigation, and strong site staff relationships at each visit, reflecting our commitment to personalized service and quality.

  • Conduct of Visits

    Vanguard CRAs conduct pre-study visits, site initiation visits, routine monitoring visits, and close-out visits with GCP/ICH principles in mind and ensuring protocol compliance, risk mitigation, and strong site staff relationships at each visit, reflecting our commitment to excellence and adherence to regulatory standards.

  • Risk Mitigation through CTMS

    Vanguard CRAs utilize CTMS to provide real time data to the Sponsor relating to milestones, action items, issues, tasks, and enrollment status, allowing the whole study team to determine risks to the success of the study throughout the lifecycle, reflecting our commitment to transparency and efficiency.

  • Site Relationship Management

    Vanguard CRAs are experts in site management, ensuring that issues at sites are addressed promptly and thoroughly, allowing sites to work efficiently and accelerate data quality, reflecting our commitment to partnership and excellence in clinical trial execution.