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A state-of-the-art outpatient Urology facility in the new Memorial Hermann Medical Plaza Building in the Texas Medical Center, is looking for an experienced Research Coordinator. The research coordinator ensures the compliance of clinical research studies and the management of protocols, ensuring accuracy and timely collection and documentation of data and safety of study volunteers. Must have at least 2 years experience as a Research Coordinator.  Urology experience a plus! Must be a Medical Assistant. Monday-Friday 8am-5pm.ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:  *Work closely with the Administrative Director, Principal Investigator and Sponsor assessing logistics, resources and costs of implementing clinical study protocols.  Serve as the primary liaison between the physician, sponsor, IRB, patient and site(s).*Understand the legal requirements and obligations of the contract and budget.*Perform regulatory management of clinical studies, including IRB submissions and coordinating all regulatory compliance for start-up and throughout the term of the study. *Timely submit the necessary documentation to the IRB to comply with FDA and other regulatory agencies. *Administer clinical studies adhering to protocol requirements and schedule of events.    *Work closely with the Administrative Director on the accurate billing of procedures performed on study.  Verify patient insurance and assess patient coverage for standard of care procedures required on the study. *Initiate study advertising for recruitment and interview potential subjects to determine eligibility. Educate patients in significant requirements and aspects of study as well as the informed consent and the procedures not covered under research.*Schedule patient visits and required testing with appropriate facilities.  *Perform patient care activities such as vitals, blood draws, specimen collection and processing, and administration of medications.*Track patient progress and maintain and document pertinent patient records and study data, according to HIPPA guidelines, informing the principal investigator of results and obtain appropriate sign-off by the PI.  Timely submit patient data to sponsor as required.*Coordinate and track the payment of stipends to patients.          *Provide backup support when requested for the physicians and nursing staff during clinic hours. Assist physicians with treatment room examination and procedures, schedules tests and appointments, answers patients calls, writes orders, records and communicates information to referring physicians and patients.Benefits once position goes direct; medical, dental and PTO.Must have:High School DiplomaPrefer Urology experienceMedical AssistantDemonstrated knowledge of medical terminology, human anatomy and physiology, and disease process.Must have strong organizational, analytical and communication skills.  Demonstrated ability to work well with a variety of people while juggling multiple tasks. Must be able to work as a team player. Knowledge of basic computer operationsBilling and insurance verification Vitals, blood draws, specimen collection and processing, and administration of medications. Highly prefer:A BA or Master’s degree with research experience Credentialed CRC (Certified Research Coordinator)