The CRC is responsible for, and critically important to the overall operational management of clinical research activities. The CRC has direct responsibility for implementing a diverse portfolio of research activities for one or more studies which may include multicenter clinical trials (both NIH and industry-sponsored), local investigator-initiated clinical trials, and/or programmatic clinical research activities, such as a clinical database and biorepository. In this role, you will be responsible for close collaboration with the Principal Investigator (PI) of each study, to facilitate timely study progress reporting to the PI and enabling appropriate PI oversight, study management, including development of source worksheets and documents and safe and accurate completion of protocol required procedures in accordance with standard operating procedures, governing regulations and study documents. You will also be performing drug accountability, patient management, including recruitment, patient interfacing, enrollment, and scheduling as well as regulatory management. The CRC works with Principal Investigators, Sub-Investigators, support staff, federal and state agencies, industry partners, and other collaborative departments to coordinate and manage investigator-initiated and sponsor-initiated clinical trials and research endeavors. This includes the responsibility for research assessment and patient intervention under the supervision of the Principal Investigator. Salary Range:$24.28-$48.04 Hourly

* A bachelor’s degree in Science or related fields strongly preferred * Demonstrated working knowledge of current medical terminology to accurately read entries in patient charts and record accurately and timely, information into study records and other appropriate research data forms. * Clinical research experience, with in depth knowledge of respective therapeutic area as it pertains to clinical trials and studies. * Demonstrated knowledge of "good clinical practices" for clinical research as defined by ICH and FDA. * Demonstrated organizational skills to efficiently and effectively provide data management/monitoring support for multiple clinical trials and projects, providing accurate information in a timely manner. * Demonstrated understanding of confidential information, how it is defined, and demonstrated skill in maintaining confidential status of such information. * Demonstrated ability to prioritize workload to meet demands of PI’s, Sponsor and FDA. * Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, , etc. * Demonstrated interpersonal skills to work with patients, their families/ guardians, physicians, administrators, work colleagues, representatives from sponsors and others to achieve maximum efficiency in reaching and maintaining workplace goals in a professional manner.