Quality is our hallmark. This is exemplified by our full-time Regulatory Specialists and Budget/Contract Associates, who are dedicated to ensure timely study start up for each of our research sites.
Timely participant recruitment is attained by our full-time Recruitment Specialists who follow a rigorous pre-screening method to ensure we enroll qualified participants. This endeavor is underscored by our high retention rates of 98%.
Our investigators specialize in a variety of therapeutic areas. They are board-certified and Good Clinical Practice (GCP) trained. In addition to regular certification, our study investigators undergo extensive training to ensure that we achieve protocol objectives, meet proposed timelines, and PI oversight. Collectively, our investigators have participated in over 500 clinical studies in Phase 1 through Phase 4. We adhere to the principles of beneficence, respect, and justice with high emphasis on ethical treatment of all our patients.
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