Clinical Sciences Intermediate Professional (Part-time, 0.4 FTE)

University of Colorado • Aurora, CO

6d • Onsite

About The Position

Intermediate Clinical Science Professionals perform clinical research-related functions, including patient-oriented research and research involving human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or the development of new technologies. Intermediate Clinical Science Professionals may also assist with epidemiologic and behavioral studies, outcomes research, and health services research. This part-time (0.4 FTE) Clinical Sciences Intermediate Professional in the CU Nursing Office of Research and Scholarship supports assigned faculty members in a driven, engaged manner through a variety of ongoing studies and research projects in the clinical/hospital setting .

Requirements

• Bachelor’s degree in any field
• One (1) year of clinical research experience or related experience
• Substitution: A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year-for-year basis.
• Applicants must meet minimum qualifications at the time of hire.
• Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
• Ability to communicate effectively, both in writing and orally
• Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
• Outstanding customer service skills
• Knowledge of basic human anatomy, physiology, and medical terminology
• Ability to interpret and master complex research protocol information
• Outstanding organizational skills and attention to detail
• Ability to represent the University in a professional and positive manner
• Ability to collaborate as a member of a team and to work highly independently to meet competing demands
• Innovative problem-solving skills and ability to thrive on challenges encountered in a fluid, complex environment
• Knowledge of institutional and governmental research administration policies and procedures, and ability to strictly follow IRB, FDA, and HIPAA regulations
• Proficient use of computers and relevant software and database applications, including REDCap, OnCore, Microsoft Office, as well as the ability to master new software programs
• Excellent project management, organizational, and time management skills

Nice To Haves

• Bachelor’s degree in science or health related field
• Two (2) years of clinical research or related experience
• Experience with electronic data capture systems (e.g., EMR or EHR and data management systems such as RedCap and/or Atlas.ti)
• Experience with quantitative and/or qualitative research and relevant software

Responsibilities

• Assist with and oversee the day-to-day operations of clinical trials and studies
• Obtain the study subject’s medical history and current medication information, review the research protocol inclusion/exclusion criteria, and confirm the eligibility of the subject to participate in the clinical trial
• Perform the informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required
• Interview prospective subjects for a variety of research clinical trials.
• Educate potential subjects on the details of the studies through phone contacts and personal interviews
• Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
• Collect, code, and analyze data obtained from research in an accurate and timely manner
• Adhere to research regulatory standards
• Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures, and other regulatory guidelines
• Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre-screening/screening activities
• Ensure that the necessary supplies and equipment for studies are in stock and in working order
• Independently master study materials, including but not limited to protocols, informed consent forms, and all other essential study documents for assigned studies
• Independently perform study-related processes, procedures, and assessments as defined in the study protocol and in compliance with regulating bodies
• Assist Team Leads, Supervisors, and/or management with the creation and implementation of processes and procedures and quality improvement initiatives
• Act as a Primary Coordinator on multiple trials/studies
• Assist and train junior team members
• Serve as gift card manager for grants
• Conduct supervised statistical coding/programming

Benefits

• The University of Colorado provides generous leave, health plans, and retirement contributions that add to your bottom line.
• Total Compensation Calculator

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees