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- info@axiommed.org
- 13151 Emily Rd. Suite 200 Dallas, TX 75240
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Our Team
Our principal investigators are specialists in the areas of Cardiology, Neurology, Sleep Medicine, Nephrology, Psychiatry, and other medical disciplines, allowing our site to support a wide range of therapeutic indications. Their diverse clinical expertise ensures accurate patient evaluation, precise diagnosis, and high-quality medical oversight throughout each study.
The research coordinator has several years of experience in conducting clinical trials and is highly skilled in participant recruitment, informed consent, protocol compliance, data collection, and source documentation. Our regulatory specialist ensures strict adherence to FDA, ICH-GCP, and institutional guidelines, maintaining accurate documentation, timely submissions, and audit-ready regulatory binders.
Our team maintains ongoing training in Good Clinical Practice (GCP), human subject protection, and study-specific protocols to ensure continuous compliance with regulatory and sponsor expectations. Regular internal meetings, staff training sessions, and quality assurance reviews are conducted to promote consistent performance, identify areas for improvement, and ensure that all study activities are conducted with accuracy, accountability, and efficiency.
The research coordinator has several years of experience in conducting clinical trials and is highly skilled in participant recruitment, informed consent, protocol compliance, data collection, and source documentation. Our regulatory specialist ensures strict adherence to FDA, ICH-GCP, and institutional guidelines, maintaining accurate documentation, timely submissions, and audit-ready regulatory binders.
Our team maintains ongoing training in Good Clinical Practice (GCP), human subject protection, and study-specific protocols to ensure continuous compliance with regulatory and sponsor expectations. Regular internal meetings, staff training sessions, and quality assurance reviews are conducted to promote consistent performance, identify areas for improvement, and ensure that all study activities are conducted with accuracy, accountability, and efficiency.
In addition, our supporting staff includes trained nurses, medical assistants, and laboratory personnel who provide high-quality clinical care and ensure precise sample handling, processing, and storage. Together, our multidisciplinary team works collaboratively to uphold the highest standards of patient safety, data integrity, and operational excellence throughout every phase of the study.
We emphasize a patient-centered approach in all our research activities. Clear communication, ethical conduct, and compassionate care are fundamental to how our team interacts with study participants. This approach has consistently resulted in strong enrollment performance, high participant retention, and positive feedback from sponsors and monitors.
Through collaboration, experience, and a shared commitment to excellence, our team is well-equipped to manage studies efficiently, meet enrollment targets, exceed sponsor expectations, and deliver reliable, high-quality data for every clinical trial we undertake.
We emphasize a patient-centered approach in all our research activities. Clear communication, ethical conduct, and compassionate care are fundamental to how our team interacts with study participants. This approach has consistently resulted in strong enrollment performance, high participant retention, and positive feedback from sponsors and monitors.
Through collaboration, experience, and a shared commitment to excellence, our team is well-equipped to manage studies efficiently, meet enrollment targets, exceed sponsor expectations, and deliver reliable, high-quality data for every clinical trial we undertake.