Posting Description: Duties for this position include but are not limited to: -Manage several clinical trials with human research subjects -Participate in the study start-up and study implementation activities -Track and report study and patient enrollment efforts and status -Participate in data quality assurance activities -Schedule and manage visits for patients enrolled in clinical trials. The main focus of this position will be an MRI outcome study implementing patient-reported outcomes and abstracting information from consented subject's electronic medical records (EPIC). Applications are accepted electronically at www.jobsatcu.com, refer to job posting RF00788 Review of applications will continue until the position is filled. Salary is commensurate with skills and experience. The University of Colorado offers a full benefits package. Information on University benefits programs, including eligibility, is located at http://www.cu.edu/pbs/. The University of Colorado Denver is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees. The University of Colorado strongly supports the principle of diversity. We encourage applications from women, ethnic minorities, persons with disabilities and all veterans. The University of Colorado is committed to diversity and equality in education and employment.
Minimum Qualifications: Position requires bachelor's degree in biological science or nursing and a minimum of 1 year fulltime experience in a clinical or healthcare setting. Education (or a combination of education and experience) may be substituted on a year by year basis for experience. Applicants must have outstanding interpersonal skills, great attention to detail, work with colleagues and patients in a confidential and professional manner, experience with web-based tracking systems and Microsoft Office programs (i.e. Excel, Word, PowerPoint and Access), and must be able to work well within a larger team.
Required Competencies/Knowledge, Skills, and Abilities:
Desired Qualifications: Experience with completing documentations and performing tasks routinely used in clinical trials, experience with performing venipunctures and EKGs. ACRP or SoCRA certification as clinical research coordinator.
Campus: Anschutz Medical Campus