Open Rank (Entry – Senior) Research Services Clinical Science Professional

University of Colorado•Colorado Springs, CO

3d•$49,899 - $78,665•Hybrid

About The Position

The Department of Emergency Medicine is seeking applications for a Open Rank (Entry – Senior) Research Services Clinical Science Professional. This is a full-time, University staff position to support ongoing grant-funded studies focused on mental health and firearm storage. The Clinical Science Professional will join a highly collaborative and exciting multi-disciplinary team (PI: Dr. Ian Stanley, PhD) that has an active research program domestically and internationally. The PI conducts research related to the prevention of psychological health conditions (e.g., suicide, posttraumatic stress disorder) across various populations (e.g., military service members, veterans, first responders, civilians). This research involves observational studies and interventional trials related to the understanding and prevention of psychological health morbidities. This position will focus on projects related to lethal means safety in veteran/military populations. This position requires familiarity and experience with clinical or public health research, preferably in psychological health and/or behavioral health. The ideal candidate will have experience within research (clinical or behavioral), collaborate effectively on multidisciplinary teams, and be highly detail oriented.

Requirements

Bachelor’s degree in any field
One (1) year clinical research or related experience
Two (2) years clinical research or related experience
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor’s degree on a year for year basis.
An advanced degree (Masters or PhD) may be substituted for experience on a year for year basis if the degree is in a field of study directly related to the work assignment.
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 medical terminology
Ability to interpret and master complex research protocol information
Excellent written and oral communication skills
Excellent organizational and interpersonal skills
Ability to think creatively, adapt quickly and work independently
Excellent team player
Self-starter with a desire to improve human health through research
High Level Skills with Computer-Based Tools (Word, Outlook, PowerPoint, Etc.)
Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future.

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)
Three (3) years of clinical research or related experience
Experience conducting qualitative interviews
Experience with survey design
Master’s degree in psychology, public health, behavioral health, or a research-related discipline
Strong interest or previous experience working in psychological health, public health, or behavioral health

Responsibilities

Assist with and oversee the day to day operations of clinical trials and studies
Review research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial
Perform informed consent process or ensures 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
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 study protocol and in compliance with regulating bodies
Assist Team Leads, Supervisors and/or management with 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
Assist with developing or develops protocol-specific systems and documents including process flows, training manuals, Standard Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies
Assist with identifying issues related to operational efficiency and shares results with leadership
Collect information to determine feasibility, recruitment and retention strategies. Employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention
Serve as a resource and participate in study initiation and close out duties
Conduct qualitative interviews
Design surveys