Research Coordinator

Where

Phoenix, AZ

What you'll be doing

This position coordinates a variety of research projects and will work independently in the acquisition of specimens, extraction of data from patient charts, and analysis of data per protocol as well as administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, and regulatory agency requirements and specific institutional requirements. The Research Coordinator ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP), and Good Clinical Practices (GCP) guidelines, which includes the following duties. Completes all tasks required by study sponsors. Coordinates the process for opening new studies. Reviews monthly financial reports, including study participant billing, expenditures, and revenue. Prepares budget analysis form according to study protocol procedures. Participates in recruitment and selection of medical study participants by interviewing and reviewing medical history to determine compliance with eligibility requirements. Coordinates and schedules a variety of medical tests including, but not limited to, blood draws, blood pressure readings, imaging studies, and cardiac and/or pulmonary function tests, as needed to establish initial patient baselines for study. Provides patient education regarding the study-to-study participants and families to ensure understanding or proper medication dosage, administration, and disease treatment. Maintains inventory level of all supplies and equipment, initiates requisitions for replacement items, and maintains equipment to provide for continuous operational efficiency. Participates in a variety of professional development programs to ensure understanding of most current methodologies, practices, and philosophies as applied to the relevant patient population and research area. Performs miscellaneous job related duties as requested.

What your background should be

One year of research experience or equivalent (Required). Certified Clinical Research Coordinator or equivalent (Preferred). Clinical Research Training Certification (Preferred)

Required Schooling / Training

Bachelor degree in related field (Required). Master degree in related field (Preferred)

Who is the client company

Its a freestanding childrens hospital

If you are interested in this position, send your resume to apply@kochdavis.com