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JTA excels in project management, clinical monitoring, clinical audits (on and off site, regulatory and data), training programs, data management services, full site management (CRA) and site coordination (CRC). We have developed extensive training programs which we can custom fit to the clients needs. We offer both junior and senior level staffing to better meet the exact work load demand and the budget of the given client. We have a strong history of covering services for trials with 50 or more sites (US, Canada and Europe), but will also help you with staffing for small projects or in-house duties. The majority of our work force is regionally located to better meet the rigors of site monitoring, both from a budget perspective and from a "burn out" perspective for the individual personnel. We have not missed a deadline in nine (9) years and will ensure your timeline is our timeline. The major portion of our workload is in device trial monitoring and auditing, however, approximately 35% of our workload is in pharmaceutical trials. We are also very experienced in Drug/Device combination trials. Our staff is trained in CNS, oncology, multiple implant types (device), laser, hearing aid, transplantation, cardiovascular, radiology, neonatal, OB/GYN, HTN, AIDS, incontinence (device), renal dialysis, BPH, IBS, GERD, arthritis and septic shock.
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