Our uniquely qualified team brings you experience in site management both within a traditional trial delivery model, as well as in expert management of a decentralized trial site solution.

Site Management & Monitoring

As clinical studies employ greater eClinical and DCT methodologies, site management and clinical monitoring processes need to become more specialized to ensure quality outcomes.

 Medtryx understands the complexities involved in managing both traditional and decentralized clinical sites, and can effectively de-risk your clinical study.

Our Site Management and Monitoring Services:

  • ICH/GCP, Global and Local regulatory compliance

  • Site Selection and Feasibility

  • Efficient site start up

  • Oversight of HREC/IRB/HA submission and approval process

  • Site Training

  • Recruitment planning and management

  • Routine site monitoring:

    • Remote monitoring visits

    • Onsite monitoring visits

  • Ongoing Source Data Verification

  • Site support for timely data query resolution

  • Drug management and accountability

  • eTMF and study documentation management

Our Site Managers form an integral part of the Medtryx clinical trial delivery team, and work to ensure your project is conducted in line with the highest quality standards.

Whether you are looking to outsource your full clinical study, only a few distinct functions or need expert advice, Medtryx will work with you to understand your specific needs and provide you with a tailored solution.