He also holds a patent for a unique syringe design. In topics ranging from management of endophthalmitis and ocular tumors. He has also co-edited a textbook and contributed chapters He is board-certified in ophthalmology as well as being a member of the American Academy of Ophthalmology and the Association for Research in Vision and Ophthalmology. HeĪlso holds master degrees in Clinical Ethics, Management of Information Technology, Data Analytics and Quantitative Analysis at the University of Virginia and Northwestern University. Lee attended Georgetown University for both undergraduate work and medical school as well as Albany University and Tulane University for Ophthalmology and Vitreoretinal fellowship with Dr. scribing, VFQ, IOP, etc.)Ĭollects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframeĬonducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the studyĪssures that amended consent forms are appropriately implemented and signedĪcts as a secondary reviewer to provide oversight so that the ICF process is conducted accuratelyĬollects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract.Dr. Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accuratelyĮfficiently completes all study tasks delegated to them (i.e. Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections protocol, ICF, manuals, etc.) and that the training is documentedĬreates, manages, and maintains source documents for each trialĪttends teleconferences and Investigator Meetings as requested by research director Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on handĮnsures study staff is properly trained on study-related information (i.e. #RETINA CONSULTANTS OF HOUSTON TRIAL#We are committed to creating an inclusive work environment that celebrates diversity.įacilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the studyĪdminister sponsor required questionnaires (i.e. Retina Consultants of Texas is proud to be an Equal Employment Opportunity and an Affirmative Action Employer. Retina Consultants of Texas follows all CDC and local authority protocols to ensure the safety and well-being of the patients, providers, employees and communities. Our surgeons have studied at some of the most renowned institutions in the nation and all have graduated at the very top of their classes. In addition, RCT has an ocular oncology division, which focuses on cancer treatments for the eye. All Retina Consultants of Texas physicians are board certified by the American Board of Ophthalmology and specialize exclusively in diseases and surgery of the retina, vitreous, and macula. RCT has three certified research centers and is home to the Greater Houston Retina Research Center, one of the country’s leading sites for retinal research. Retina Consultants of Texas is one of the largest and most respected retina-only ophthalmology practices in the United States, committed to Preserving the Patient's Vision. Through RCA's physician-centered practice management model, physicians continue to drive clinical and practice culture while benefiting from the available business expertise, resources and shared best practices. Retina Consultants of Texas is part of Retina Consultants of America (RCA), the largest network of leading retina specialists with the mission of saving sight and improving patient lives through innovation and the highest quality care. RCTX offers the following competitive benefits for full-time eligible employees after the introductory period: #RETINA CONSULTANTS OF HOUSTON MANUAL#The Research Study Coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Retina Consultants of Texas (RCTX) is seeking a Research Study Coordinator to join our growing Research team.
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