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SynteractHCR’s medical monitors are experienced clinicians and clinical research experts who work as part of your team and are available to you 24 hours a day, if necessary, so you can be comfortable that your study is covered by a physician you can trust and who is available to you any time.
Our team includes MDs across therapeutic areas that are available to provide medical expertise to guide your clinical development needs. They provide medical consultation to investigational sites and the rest of the project team, including responses to questions regarding inclusion/exclusion of patients, review of lab data, and physician review of SAEs. They are experienced in working with Data Safety Monitoring Boards (DSMBs) and Data Monitoring Committees (DMCs).
Our physicians have the experience and expertise to help you with protocol development, development of global safety plans, and regulatory submissions. SynteractHCR medical monitors work seamlessly with our safety surveillance group to prepare the client-specific or study-specific global safety plan for SAEs and with the SynteractHCR medical coding group to establish study-specific coding conventions for SAEs, AEs, and concomitant medications.
With backgrounds and specialties that cover the range from small Phase I studies to larger international studies, our medical monitoring support flexes to fit your needs. Our highly experienced team enables seamless coverage for studies.