Job Information
Children's Hospital Colorado Clinical Research Assistant Multidisciplinary in Aurora, Colorado
Apply for Job
Job ID87764
LocationAurora, Colorado
Full/Part TimeFull-Time
Regular/TemporaryRegular
Add to Favorite Jobs
Why Work at Children's....
Here, it's different. Come join us. Children's Hospital Colorado has defined and delivered pediatric healthcare excellence for more than 100 years. Here, the nation's brightest nurses, physicians, scientists, researchers, therapists, and care providers are creating the future of child health. With an optimist's outlook, a trailblazing spirit, and a celebrated history, we're making new strides every day. We've been Magnet-designated four times by the American Nurses Credentialing Center and are consistently recognized among the best of the best pediatric hospitals with #1 rankings in Colorado and the region by U.S. News & World Report. As a national leader in pediatric care, we serve children and families from all over the nation. Our System of Care includes four pediatric hospitals, 11 specialty care centers, 1,300+ outreach clinics and more than 10,000 healthcare professionals representing the full spectrum of pediatric care specialties. Here, we know it takes all of us, every role, to deliver the best possible care to each child and family we treat. That's why we build our teams toward a foundation of equity in access, advancement, and opportunity. We know teams of individuals with different identities and backgrounds can nurture creativity and innovation. We know we can see, treat, and heal children better when our team reflects the diversity of our patient population. We strive to attract and retain diverse talent because we know a truly inclusive and equitable workforce will help us one day realize our most basic calling: to heal every child who comes through o A career at Children's Colorado will challenge you, inspire you, and motivate you to make a difference in the life of a child. Here, it's different.
Job Overview
The Clinical Research Assistant is responsible for providing administrative support for the day-to-day operations of assigned clinical research programs and/or studies conducted by Principal Investigators (PIs) at the University of Colorado Anschutz Medical Campus. Performs a variety of administrative duties involved in the collection, compilation, documentation and review of clinical research data. Supports the achievement of research program and/or study objectives. Works under close and direct super
Additional Information
Department: Research Institute Hours per week: 40, eligible for benefits Shift: Monday - Friday, 8am to 4:30pm. Work hours may vary due to department needs.
Qualifications
Education: High school diploma or equivalent is required.
Responsibilities
POPULATION SPECIFIC CARE Neonate - 30 days to 1yr Toddlers - >1yr to 3yrs Pre-Schoolers - >3yrs to 5yrs School age - >5yrs to 13yrs Adolescent - >13yrs to 18yrs Adult - >18yrs to 65yrs ESSENTIAL FUNCTIONS An employee in this position may be called upon to do any or all of the following essential functions. These examples do not include all of the functions which the employee may be expected to perform. Assists regulatory team with Institutional Review Board (IRB) preparation and submission, including collation and preparation of documents. Screens and schedules participants in a variety of clinical research programs and/or studies. Consents subjects and/or families for registry or non-interventional research studies. Prepares for and takes part in site initiation, monitoring, closeout visits, and document storage activities. Conducts and documents visits and testing/interviews according to all regulatory and organizational protocols. Collects, prepares, processes, ships and maintains inventory of research specim Maintains subject level documentation and prepares documents, equipment and/or supplies. Provides input for and assists with developing IRB related documents. Collaborates with coordi ating staff to maintain appropriate documentation. Assists to identify issues related to operational efficiency and shares results with supervising coordinator staff and/or management. Maintains compliance with institutional requirements and policies. Maintains a familiarity with the ethical conduct of research and safeguards needed when conducting clinical research. Participates in sponsor-required training. Participates in team meetings.
