Summary The Cystic Fibrosis (CF) Clinical Research team at National Jewish Health is seeking an Assistant Clinical Research Coordinator to support a wide range of adult CF research studies, from genotype-specific investigational products to observational studies on pregnancy in women with CF. Thanks to advancements in care driven by research, people with CF are living well into adulthood. Our team plays a key role in this progress, offering a dynamic environment with opportunities to develop and apply a variety of clinical research skills. We’re looking for someone who is positive, organized, collaborative, and eager to learn. Procedures commonly performed by the team include: Pulmonary function testing Nasal brushing/curettage Sputum induction and collection Nasal potential difference Macroduct sweat collection Phlebotomy Key responsibilities include: Study recruitment and enrollment Coordinating simple to complex study visits Maintaining investigator site files Specimen processing, shipping, and data entry IRB submissions and documentation This role works closely with clinical teams and physician investigators and is a valued part of both the clinical and research communities. Prior CF experience is not required. This is an exciting time in CF research, with new treatments on the horizon and opportunities for professional growth through writing, speaking, and conference attendance. As the leading respiratory hospital in the nation, National Jewish Health is advancing personalized medicine through exceptional care, education, and research. Position Summary The Assistant Clinical Research Coordinator will work with a preceptor to learn the regulations, guidelines and institutional policies that govern the proper conduct of research at National Jewish Health and learn to manage the operational aspects of clinical research. Essential Duties Learns and applies Clinical Research Guidelines including Good Clinical Practice, HIPAA regulations, CRS Standard Operating Procedures, applicable NJH Policies and Procedures, and FDA, NIH, OHRP, ICH guidelines as applicable. Masters all study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies. Learns and performs study-related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies and NJH competency requirements. Complies with regulatory bodies to create and maintain study records, and if applicable, dispensation and accountability of investigational product.
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Job Type
Full-time
Career Level
Entry Level